- About this Journal ·
- Abstracting and Indexing ·
- Aims and Scope ·
- Annual Issues ·
- Article Processing Charges ·
- Author Guidelines ·
- Bibliographic Information ·
- Citations to this Journal ·
- Contact Information ·
- Editorial Board ·
- Editorial Workflow ·
- Free eTOC Alerts ·
- Publication Ethics ·
- Recently Accepted Articles ·
- Reviewers Acknowledgment ·
- Submit a Manuscript ·
- Subscription Information ·
- Table of Contents
BioMed Research International
Volume 2013 (2013), Article ID 121684, 10 pages
Illuminating the Petite Picture of T Cell Memory Responses to Listeria monocytogenes
1Interdisciplinary Biotechnology Unit, Aligarh Muslim University, Aligarh, Uttar Pradesh 202002, India
2Women’s College, Aligarh Muslim University, Aligarh, Uttar Pradesh 202002, India
Received 17 June 2013; Accepted 25 July 2013
Academic Editor: Anshu Agrawal
Copyright © 2013 Saba Tufail et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
The ease to culture, moderately less safety constraints in handling, and above all, hurdle free induction of an anticipated infection in mouse rendered Listeria monocytogenes the rank of a model organism for studying a variety of host immune responses. Listeria monocytogenes being an intracellular pathogen evokes potent CD8 T cell response during which CD8 T cells pass through a massive expansion phase. This is generally followed by contraction phase wherein majority of activated cells undergo apoptosis leaving behind a population of memory CD8 T cells that has potential to confer enhanced protection upon reencounter with the same pathogen. Functional attributes of various cytokines, transcription factors, receptors, adaptors, and effectors pertaining to the generation of robust memory T cell response have begun to be unravelled for better understanding of memory and opening avenues to create superior vaccine strategies. This review is an attempt to unveil related discoveries along with updating recent advances on this issue.
Listeria monocytogenes is a Gram-positive facultative intracellular bacterium and the causative agent of listeriosis, the most pernicious amongst various food borne infections in humans accounting for about 20–30% deaths worldwide . Listeriosis is characterized by systemic dissemination of the heavy ingested inoculum of bacteria from gut to systemic circulation to various organs including brain manifesting in the establishment of gastroenteritis, septicaemia, and meningoencephalitis. Moreover, Listeria monocytogenes has a profound predilection for disseminated infection during pregnancy [2–4] which is attributable to the induction of fetal-placental infection triggering stillbirth, spontaneous abortion, premature delivery, and neonatal infection .
Listeria monocytogenes disseminates infection by cell-to-cell mode of spread along with being endowed with the capability of infecting both nonprofessional phagocytes (gut epithelial cells) and professional phagocytes (macrophages) . The notoriety of the pathogen is associated with its ability to make macrophage cytosol its replicative niche , and it does so by disrupting the internalization vacuole exploiting its pore forming toxin, listeriolysin O (LLO), curtailing the fusion of the vacuole to hydrolytic phagosome . The cytosolic abode and cell-to-cell spread protect the pathogen from extracellular milieu and safeguard it against antibody onslaught and complement attack. The intracellular niche occupied by Listeria monocytogenes leads to induction of potent CD8 T cell response wherein CD8 T cells proliferate and differentiate to effector cells in order to contain the infection. CD8 T cells play centrestage in the control and obliteration of intracellular pathogens . Moreover, dendritic cell cross-priming of CD8 T cells is of chief importance in alarming cellular immune responses to Listeria monocytogenes infection. Once the infection is eliminated, the CD8 T cell population begins to contract as the bulk of the Listeria-specific CD8 T cells undergo apoptotic cell death; therefore, a skimpy population (5–10%) of Listeria-specific CD8 T cells is left to enter the memory T cell pool, and it is this memory T cell pool that confers better protection upon rechallenge with Listeria monocytogenes . The CD8 T cell memory pool generated so forth does not carry a homogenous population rather a heterogeneous one which can be separated into central memory T cells (TCM) carrying high proliferation capacity but reduced immediate effector function and effector memory T cells (TEM) carrying low proliferation capacity but profound immediate effector function [9–13]. The heterogeneous CD8 T cell memory population is based on the expression of CD62L and CCR7; TCM is and CCR7+ while TEM is and CCR7− .
The focal point of this review is T cell memory response to Listeria monocytogenes infection, and the reason behind choosing Listeria monocytogenes as the centrestage organism for this review is its exploitation as a model organism to study immune response against intracellular pathogens, and this is owed to the genetic manipulability of this microorganism and availability of overwhelming information on its pathogenesis [6, 15]. Exploiting the mutability of Listeria monocytogenes, its avirulent strains have been created which however retain the capacity to induce potent and protective acquired immune response and help deciphering a wider scope of immune response to intracellular pathogens .
Herein, first we detail the generation of memory T cells in response to Listeria monocytogenes infection enumerating the “models” proposed for their differentiation. Second we review the role of various cytokines, transcription factors, receptors, adaptors, and effectors in the generation of a robust CD8 T cell memory response along with highlighting the recent breakthroughs. Further, we discuss the contribution of CD4 T cells and B cells in generation and maintenance of CD8 T cell memory response. Lastly, we enumerate how understanding memory response opens avenues for development of better vaccines. Figure 1 gives an overview of the factors playing crucial roles in generation of memory CD8 T cells.
2. Generation of Functional Memory CD8 T Cells
2.1. Models of Memory CD8 T Cell Generation
It is very well documented that CD8 memory T cells play an indispensable role in controlling intracellular pathogens like viruses and certain bacteria including Listeria monocytogenes. As already discussed, postelimination of primary infection, the host harbours two distinct CD8 T cell memory subpopulations: TEM and TCM. Two conflicting models for memory T cell differentiation have been proposed: one being “linear differentiation model” and the other being “progressive differentiation model.” According to linear differentiation model, memory T cells develop in continuum from naive cells which get activated upon antigen encounter and give rise to TEM which finally progress to TCM. TCM represents the memory T cell subpopulation that confers enhanced protection upon reencountering the same pathogen [16, 17]. The progressive model describes that TCM generation bypasses the TEM stage and arises directly from naive cells [16, 18]. According to this model, the “signal strength” to TCR (T cell receptor) during priming and expansion phase determines the fate. It is proposed for this model that, as a consequence of strong activating signal strength, T cells acquire full effector function and lose their potential to proliferate and survive. TCM is generated in response to weak signals and provides precursors for rapid generation of antigen-specific effector cells, whereas TEM has been proposed to develop as a consequence of intermediate signal strength. A study conducted by Teixeiro et al.  showed results falling in line with the progressive model. They have demonstrated that it is the differential TCR signaling in Listeria monocytogenes infection which determines CD8 T cell memory versus effector development. They exploited a mutant TCR transgenic model infected with Listeria monocytogenesand found that point mutations in the TCR β transmembrane domain although could not impact primary effector CD8 T cell response, they ensued in impaired development and function of CD8 memory T cells.
Different experimental systems and methods used to define phenotype and purify T cell subsets have been attributed for the existence of such contrasting views . Problems with infection models have also been proposed to be the cause of deviating views, as in the case of chronic persistent viral infections; details about potential in vivo antigen (re) exposure are not clear, and frequent antigen encounters may increase the diversity of expression patterns for some markers . Since linear model is often taken into account while describing antigen-specific T cell memory response, the details summarized herein are majorly in the light of this model.
2.2. Functional Avidities and Differentiation of Memory CD8 T Cells
High functional avidities determine the differentiation and longevity of memory T cells to accomplish the memory program. In an earlier study, Listeria monocytogenes specific effector and memory CD8 T cell populations have been investigated with respect to TCR repertoire . The heterogenous CD8 T cell population (effector and memory CD8 T cells) comprises cells specific for immunodominant epitopes and expressing a broad spectrum of TCRs. Interestingly, TCR repertoire expressed during the primary response is retained by the memory T cells. However, during clonal expansion of memory T cells after reinfection with Listeria monocytogenes, the broad spectrum of TCR repertoire is narrowed rendering development of T cells carrying higher avidity for antigen. It is quite feasible that higher avidity memory T cells would have selective advantage on rechallenge, but the comprehension of precise mechanisms rendering alteration of TCR remains elusive. Furthermore, in a recent study, some researchers have also investigated whether CD8 T cells stimulated by low affinity ligands give rise to memory T cell population . They chose a model in which TCR transgenic OT-1 cells were stimulated by five different altered peptide ligands (APLs) which were derivatives of original OT-1 ligand SIINFEKL (N4) and differed in the potency to stimulate OT-1 cells. Mice were infected with recombinant Listeria monocytogenes strains expressing chicken Ova protein containing APL (Listeria monocytogenes-APLOVA) in place of the N4 epitope. After 138 days of OT-1 cell stimulation by various APLs, a finite population was found to remain stable. Recombinant vesicular stomatitis virus expressing Ova (VSV-N4OVA) challenge rendered significant expansion of the OT-1 cells previously exposed to any of the APLs. On the contrary, far fewer OT-1 cells were observed after VSV-N4OVA challenge in mice that initially received a wild-type Listeria infection, which suggests that all the APLs generated memory cells. Transfection of N4 and V4 memory OT-1 cells into naive hosts led to comparable expansion of both after Listeria monocytogenes-N4OVA rechallenge. Interestingly, both memory populations also responded similarly to Listeria monocytogenes-V4OVA rechallenge. Thus, not the priming antigen rather the strength of the recall stimulus determines the expansion in the recall response. The findings enumerate that even very weak TCR-ligand interactions are enough to drive the formation of functional memory T cells and support the reports indicating that lymphopenia-driven homeostatic expansion, a manifestation where T cells also encounter only very weak TCR ligands, generates functional memory T cells .
2.3. Memory CD8 T Cell Differentiation Is Rapid and a Function of Duration of Infectious Period
It has been reported that Listeria-specific CD8 T cells are present during initial days after primary immune response, and their extensive potential to proliferate after antigen reencounter indicates that memory T cells undergo rapid differentiation [22, 23]. Moreover, CD127 (also known as the IL-7R) expressing T cell subsets seemingly appear at early time points in response to Listeria monocytogenes infection which further falls in line with the notion that memory T cell development is rapid [20, 24]. Williams and Bevanhave reported that duration of infectious period of Listeria monocytogenes dictates the programming of CD8 T cells to memory T cells . Although, it is well known that brief exposure to antigen leads to expansion and differentiation of CD8 T cells, their work proves that full memory differentiation of CD8 T cells remains diminished when the infectious period is shortened. So, it appears that CD8 T cell memory programming is dependent on threshold infection duration. Furthermore, the finite size of memory CD8 T cells generated after Listeria monocytogenes infection has also been investigated because the number of memory cells formed is in direct corelation with the level of protection rendered in the infected host [17, 26–29]. Hence, seemingly a protective number of effector and memory CD8 T cells are indispensable to fight various infections and malignancies.
2.4. Cytokines and Transcription Factors Required to Generate Robust Memory CD8 T Cells
It has been spoken loud that CD8 T cell memory formation is critical for developing protective immunity against reinfection but the signals required to program activated CD8 T cells to develop into memory cells remain obscure. CD4 T cell assistance [30, 31] and IL-2 signals during priming have been reported to play some role in the establishment of memory population . A recent study supports the critical function of IL-12 and type I Interferon (IFN) in inducing CD8 T cell memory development in response to Listeria monocytogenes infection . Xiao et al.  report that, within three days of the initial phase of naive CD8 T cell expansion in response to Ag, memory development by IL-12 is completely programmed but this indoctrination does not lead to formation of memory cell population expressing killer cell lectin-like receptor G1 (KLRG1); rather the majority cells express phenotype which is an attribute of central memory cells. Hence, three major classes of signals contribute to T cell activation and their transit to memory cell development, signal 1 from antigen stimulation of TCR, signal 2 comes from costimulatory signalling through molecules like CD28, and the signal 3 is derived from the above-discussed cytokines namely, IL-12 and type I IFN. Differential expression of the T-box transcription factor, T-bet, has been revealed to partly mediate the effect of inflammatory cytokines like IL-12 on effector and memory CD8 T cells [34–36]. Moreover, downstream transcriptional programs of Wnt signalling have been reported to play as signal 4 in modulating T cell responses . Wnt proteins (secreted, lipid modified glycoproteins) regulate various cellular activities owing to their potential to activate multiple signal transduction pathways. Zhao et al. demonstrate that TCF-1 (T cell factor 1) and LEF-1 (lymphoid enhancer-binding factor 1), the effector transcription factors of canonical Wnt pathway in a manner similar to IL-7Rα and CD62L, exhibit dynamic expression changes during expansion of antigen-specific CD8 T cells in response to Listeria monocytogenes infection . They found naive T cells to express plenty of TCF-1 and LEF-1 which were however downsized in number in effector T cells but found to be upregulated again in memory T cells. The study revealed that memory CD8 T cells transitioned to a large population of secondary effectors which rendered rapid clearance of bacteria after rechallenging immunized mice with virulent Listeria monocytogenes. The finding clearly suggests that activation of the canonical Wnt pathway leads to generation of memory CD8 T cell population during initial immunization, ensuing in ameliorated protective immunity upon further challenge with the same pathogen.
TCF-1 and LEF-1 transcription factors exhibit overlapping roles in thymocyte maturation and have also been found to regulate memory CD8 T cell differentiation and persistence, but a wider spectrum of their functions remains yet to be unravelled. Zhou and Xue made an effort in this direction when they studied the effect of double deficiency of TCF-1 and LEF-1 on generation of memory precursors in effector CD8 T cell populations in response to Listeria monocytogenes infection . The double deficit totally abrogated the generation of IL- memory precursors and CD8 effectors lacking TCF-1 and LEF-1 although could still express IFN-γ, granzyme B, and perforin, but TNF-α production was found to be hampered in them. The double deficient antigen-specific CD8 T cells exhibited an effector phenotype in the memory phase, and, in secondary expansion upon reencounter, they were severely impaired. So, it can be concluded that TCF-1 and LEF-1 regulate generation of memory precursors and protective memory T cells in unison.
As already discussed, IL-12 and IFN-γ induce protective immunity against Listeria monocytogenes infection by regulating memory CD8 T cell development as well as modulating magnitude of short-lived effector cells generated. A group recently examined the role of a related cytokine, IL-23, in this regard and concluded that, in the absence of IL-12, it can act as its partial substitute for generation of protective immunity against Listeria monocytogenes challenge . Moreover, Sandau et al. demonstrated that IL-15 plays a crucial role in dictating the composition as well as maintaining the CD8 memory pool; that is, it regulates both qualitative as well as quantitative features of CD8 memory T cell population . The researchers observed that, after boosting, mice lacking IL-15 could not give rise to a subset of effector memory cells, including a population of IL-7Rα low cells which however were found to be in higher proportion among secondary memory cells in normal mice. IL-15 deficiency also induced changes within the IL- subset of secondary memory CD8 T cells, which expressed high levels of CD27 but minimal granzyme B. Moreover, including these qualitative changes, deficiency of IL-15 led to reduced cycle and impairment of Bcl-2 expression by secondary memory CD8 T cells which is indicative of a definite role of IL-15 in basal proliferation and survival of the memory cell pool. Moreover, IL-7 has also been found to regulate the differentiation of CD8 memory T cells following the effector phase .
Whereas shaping CD8 T cell memory requires some cytokines, there are others which either function conversely or leave no effect. IL-10 has been well documented for inducing downregulation of T cell responses . Moreover, Biswas et al. demonstrated that, in the absence of IL-10, primary and memory CD8 T cell responses against Listeria monocytogenes infection are enhanced . Furthermore, a little later, Haring and Harty evaluated antigen-specific CD4 and CD8 responses in the absence of IL-18 or IL-18Rα to determine the role of this cytokine in development and homeostasis of T cells. Whereas they observed a regulatory function of IL-18/IL-18Rα in CD8 T cell contraction, their experiments revealed that neither IL-18 nor IL-18Rα is required for the generation, contraction, or maintenance of memory CD4 and CD8 T cells in response to infection with an attenuated strain of Listeria monocytogenes .
2.5. Inflammatory Environment Contributes to Memory CD8 T Cell Differentiation
Pathogen induced inflammatory environment has also been observed to control effector and memory CD8 T cell differentiation . According to the differential model, short-lived effector cell (SLEC: IL- ) and memory precursor effector cell (MPEC: IL- ) are formed from an early-effector cell (EEC: IL- ). Obar et al.  demonstrated that the composition of the inflammatory environment induced by Listeria monocytogenes and vesicular stomatitis virus (VSV) infections affects effector CD8 T cell differentiation. They observed that inflammation in addition to altering SLEC/MPEC differentiation also limited the differentiation of T effector memory cells that searingly affected the functionality of the effector CD8 T cell population and composition of the MPEC population. Moreover, they found that SLEC/MPEC differentiation was altered in a memory cell intrinsic manner as a consequence of multiple encounters with the same antigen. It leads to the conclusion that effector and memory CD8 T cell differentiations are regulated by the type of priming pathogen and the number of the times the cell encounters the same pathogen.
2.6. Adaptors, Ligands, and Receptors Required to Shape CD8 T Cell Memory
The mechanisms that direct the induction and maintenance of memory T cells are not clear yet. Gads, an adaptor protein in TCR signalling, plays an indispensable role in TCR mediated Ca2+ immobilization . Effect of Gads deficiency on CD8 T cell mediated immunity has also been investigated in Listeria monocytogenes infection . During the initial phase, Gads+/+ and Gads−/− CD8 T cells expanded to an equivalent level, although the expression of CD69 and CD25 was reduced in the absence of Gads. Additionally, Gads was albeit required to sustain the proliferative phase of immune response five days after infection, it played no role in differentiation of naive CD8 T cells into memory cells.
Another study conducted by Pearce et al. reveals that TRAF6, an adaptor protein in the TNF receptor (TNFR) and IL-1R/TLR superfamily, regulates development of CD8 T cell memory following Listeria monocytogenes infection by modulating fatty acid metabolism . They found that mice with T cell specific deletion of TRAF6 could generate robust CD8 effector T cell responses which were however defective in their ability to transit to memory CD8 T cell population. Moreover, their study revealed that expression of genes regulating fatty acid metabolism is altered in TRAF6-deficient CD8 T cells. Falling in line, in the absence of growth factors, activated CD8 T cells lacking TRAF6 display defective AMPK activation and mitochondrial fatty acid oxidation (FAO). They found that administration of antidiabetic drug metformin replenished FAO and memory CD8 T cell production in TRAF6 deficient mice, and, interestingly, this treatment could also ameliorate memory CD8 T cell generation in wild-type mice.
A G protein coupled neuropeptide receptor, VPAC1 (vasoactive intestinal peptide/pituitary adenylate cyclase activating polypeptide receptor 1) has also be investigated for its regulatory role on CD8 T cells in response to Listeria monocytogenes infection . It has been demonstrated that CD8 T cells responding to Listeria monocytogenes have downregulated expression of VPAC1, so downregulation of VPAC1 expression exhibits inverse relationship with CD8 T cell proliferation. Interestingly, VPAC1 expression normalised to naive level in primary but remained low during secondary, memory generation.
According to a report, Fas death pathway has some share in modulating the function of memory CD8 T cells . While a similar increase or decrease of CD8 T cell response is observed against Listeria monocytogenes infection in wild-type (WT) and Fas ligand (FasL) mutant mice, FasL mutant mice had mainly TEM population in the long term when compared to WT mice that carried majorly TCM population. Downregulation of IFN-γ, poor homeostasis, and antigen-induced proliferation were observed for memory CD8 T cells in FasL mutant mice. Interestingly, faulty programming or defective FasL expression on CD8 T cells is not responsible for impaired CD8 T cell memory in FasL mutants, but the deranged cytokine environment in FasL mutant mice played the culprit. Although adoptively transferred WT memory CD8 T cells could confer protection against Listeria monocytogenes in either the WT or FasL mutant hosts, memory CD8 T cells in FasL mutants could not deliver protection even in WT hosts. Hence, subjects carrying mutation in Fas pathway have impaired memory CD8 T cell function which can render them susceptible to recurrent or latent infections.
2.7. Cell Cycle Regulatory Molecules Modulate the Generation of CD8 T Cell Memory
In addition to the above-mentioned regulatory mechanisms, cell cycle regulatory molecules have also been reported to be key regulators of T cell response . , a cyclin-dependent kinase inhibitor, has been found to be a critical regulator of the CD8 T cell homeostasis as well as response to an acute viral infection . Most importantly, , in addition to inhibiting the programmed expansion of IL-2 producing memory precursors, had its impact on the magnitude and quality of CD8 T cell memory. Singh et al.  observed the effect of deletion on CD8 T cell proliferation upon vaccination with recombinant Listeria monocytogenes. They found, that initially after vaccination, CD8 T cells exhibited superior recall responses in the absence of . Moreover, their study reflects an inhibitory role of in proliferative renewal of memory CD8 T cells, the effector memory subset in particular. The study indicates cell cycle regulation of CD8 T cell homeostasis and supports the idea of modulating to boost vaccine induced T cell memory as well as protective immunity.
Bcl-2, an apoptosis regulatory protein, has also been proposed to be indispensable for the survival of memory cells [47–49]. Several studies relying on double knockout models have proposed a skewing role for Bcl-2. Dunkle et al.  performed adoptive transfer experiments, a method to confirm memory potential of cell subsets, exploiting Bcl-2 as a marker which earlier could not be performed owing to the intracellular localization of Bcl-2. They used a novel Bcl-2 reporter mouse model and reported that a distinct subset of effector T cells including a subset within the - memory precursor effector cell population retains high Bcl-2 expression at the peak of the CD8 T cell response to Listeria monocytogenes. Moreover, their findings enumerate the correlation of Bcl-2 with memory potential in adoptive transfer experiments exploiting both total responding CD8 T cells and memory precursor effector cells. Their results show that Bcl-2, despite being within the memory precursor effector cell population, renders a survival advantage to a subset of effector CD8 T cells allowing their differentiation into memory cells. The findings paint a clear picture of the critical role of Bcl-2 in memory T cell generation. Diacetylated histone H3 (diAcH3) has also been reported as a useful marker for evaluating the functionality of memory CD8 T cells upon Listeria monocytogenes infection. Studies performed by DiSpirito and Shen demonstrate that memory T cells impaired in rapid recall response carry less abundant diAcH3 in comparison to their wholesome counterparts which makes diAcH3 level in memory T cells an asset to evaluate their functionality .
2.8. Kinases As Well Have Some Control over CD8 T Cell Memory Generation
AMPK, adenosine monophosphate-activated protein kinase, gets activated in response to TCR signals upon antigen encounter and during energy stress in T cells as well [51, 52]. It is well documented that AMPK can establish homeostasis and implement dormancy to put down the energy demand in many cell types . Considering these facts, Rolf et al.  investigated the role of AMPK during the contraction phase of immune response in regulating the transition of metabolically active effector CD8 T cells to the metabolically dormant catabolic memory T cells. They found that, although AMPKα1 activity is not necessarily required for proliferation and differentiation of CTLs, it becomes critical for in vivo survival of CTLs when immune stimulation is withdrawn. They show that T cells lacking AMPKα1 were critically defective in their potential to generate memory CD8 T cell responses during Listeria monocytogenes infection. Hence, their findings give an insight that AMPKα1 controls CD8 T cell memory.
3. CD4 T Cells Assist in Memory CD8 T Cell Generation
Factors affecting CD8 T cell response upon bacterial and viral infections are numerous combined with being complex. One of the factors influencing long term survival and fitness of CD8 T memory cell pool is CD4 T cell help . Infection with Listeria monocytogenes (either intravenous or enteric) induces clonal expansion of CD4 cells in a manner similar to CD8 T cells . Although assistance of CD4 T cells for the generation of CD8 T cell immune response is overruled during the primary immune response to Listeria monocytogenes infection, it plays centrestage for long term maintenance of memory CD8 T cells and establishment of protective immunity against reinfection [20, 55, 56]. Whereas reduced memory in mice lacking CD4 T cell appears only several weeks after infection, CD4 T cells have been found to be critical during the initial priming process, during which they render CD8 T cells with enormous potential to proliferate upon reencounter with the pathogen months later [20, 57]. Hence, CD4 T cell deficient environment renders development and maintenance of CD8 T memory cell pool with reduced magnitude over time affecting the ability of CD8 memory T cells to expand and perform effector functions like cytokine production and hampering their cytotoxic potential which ultimately wanes generation of protective immunity upon rechallenge with the same pathogen. Moreover, it has been demonstrated that memory maintenance stage of CD8 T cell memory requires the presence of CD4 T cells giving insight into the direct or indirect role of CD4 cells to shape the comprehensive quality and functionality of the CD8 memory T cell pool [20, 57, 58].
Though CD4 T cells have been found to impact long term memory CD8 T cells positively, contrastingly, a subset CD4 CD25 regulatory T cells (Tregs) have been found to suppress Listeria monocytogenes-CD8 T cell responses. In CD4 T cell deficient mice, enhanced memory CD8 T cell responses were observed at the time of reinfection in response to immunization, in particular, with peptides or DNA [20, 59]. When CD25 positive cells were depleted, it left a similar effect indicating an inhibitory function of Tregs on Listeria monocytogenes specific CD8 T cell responses. Interestingly, when wild-type mice are immunized with heat killed Listeria monocytogenes (HKLM), protective immunity is not conferred in them, but a higher level of protection is rendered if the mice are depleted in CD4 cells . This suggests that Tregs has a restraining effect on CD8 T cell responses following immunization with HKLM, but, on the contrary, Tregs are induced less effectively after infection with live, virulent bacteria.
However, conversely to the above report, a more recent study has unravelled an unexpected function of Tregs. The findings enumerate that Tregs deficit causes activation and expansion of a population of low avidity CD8 cells which leaves the activation of high-avidity T cells impaired during primary immune response resulting in downsized memory to Listeria monocytogenes. Considering the results, Tregs can be called critical regulators of homeostasis of CD8 T cell priming and inducers of high-avidity primary responses and effective memory .
Whereas T cell help is said to be required for the primary response, experiments with noninflammatory immunogens have demonstrated it to be required for generation of secondary response. CD4 T cell help during the initial phase (the first few days) of the immune response has been found to influence the development of a secondary response [57, 62, 63]. As the CD4 T cells are required during the initial phase to program the ensuing CD8 T cell memory response, “unhelped” CD8 T cells, that is, the cells which were not assisted by CD4 during priming, are destined to undergo “activation induced cell death” (AICD) upon restimulation. This is why upon rechallenge ill effects of priming in the absence of CD4 T cell help are seen . Sacks and Bevan  have added information with respect to CD4 T cell help. They wondered if TRAIL blockade could rescue impaired CD8 T cell memory in the absence of CD4 help as it has been reported that, in “unhelped” CD8 cells, TRAIL deficit rescues the expansion of restimulated CD8 T cells . They studied memory T cell response in mice doubly deficient in CD4 T cells and TRAIL and found reduced memory CD8 T cell pool in these mice with time and conferred lesser protective immunity upon rechallenge with Listeria monocytogenes like their counterparts which were TRAIL sufficient but CD4 unhelped. Hence, Sacks and Bevan conclude “TRAIL deficiency does not rescue impaired CD8 T cell memory generated in the absence of CD4 T cell help” .
Interestingly, a very recent study highlights that a subunit vaccine that combines polyIC and an agonistic CD40 antibody could “program” protective CD4 independent CD8 T cell memory in response to Listeria monocytogenes infection .
4. B Cells Too Have Some Part to Play in CD8 T Cell Memory Generation
Earlier, the intracellular residence occupied by Listeria monocytogenes made the scientific fraternity to conceive the notion that the humoral immune response has to play no role in the control of Listeria monocytogenes infection. However, later on, a few findings sprouted in favour of B cell, and antibody influence over Listeria monocytogenes infection put that backdrop idea to rest. As B cells have been found to play some part in the generation of T cell response and establishment of memory, they are believed to contribute indirectly in evoking anti-L. monocytogenes immunity. Binding of B cell surface and soluble antibodies to their cognate antigens in secondary lymphoid organs, where specific immune responses are initiated, can facilitate the generation of protective T cell response. Whether CD4 and CD8 T cell responses are differentially affected during B cell deficit remains obscure. A study conducted by Shen et al.  highlights that, albeit B cells perform a minimal function in the initial activation and antigen-driven expansion of CD8 T lymphocytes, their absence during the contraction phase renders increased death of activated CD8 T cells, leading to reduced Listeria-specific CD8 T cell memory. However, B cell influence on long term maintenance and rapid recall response of memory CD8 T cells is denied. Mice deficient in B cells exhibit increased contraction of antigen-specific CD8 T cells, but this possibly is not a consequence of impaired CD4 T cell responses since Listeria-specific CD4 T cell priming has been found to be normal in B cell deficient mice . Furthermore, an overcontraction of antigen-specific CD8 T cells was overruled in CD4 deficient mice. Thus, B cells are equipped to perform a specific function of modulating the contraction of CD8 T cell responses following immunization. However, the factors regulating the apoptotic phase remain yet to be unravelled but once elucidated may open avenues to manipulate this process to augment immunological memory and, thus, vaccine efficacy. Furthermore, the old proposition that antigen antibody complex retention on follicular dendritic cells influences the maintenance of long term T cell memory  was challenged by later experimental evidence [67–69]. Thus, it becomes very apparent that B cells contribute in modulating T cell responses in Listeria monocytogenes and many other similar infections.
5. Memory T Cells and Vaccine Development
As discussed earlier, antigen-specific CD4 and CD8 T cells which exist in lower frequencies in naive hosts are the key players in protective immunity. After proliferation in response to antigen, contraction phase begins in which a subpopulation of antigen specific T cells forms memory cell pool. This immunological memory is the basis for vaccination, and wholesome efforts have been put to improve vaccine design through manipulating T cell responses which would maximize memory T cell formation. Although it has been suggested that TCM has a better capacity to replenish memory T cell pool and to mediate protective immunity than TEM because of their greater capacity to proliferate and persist in vivo, the findings of Huster et al. show that TEM is crucial for providing efficient protective immunity against Listeria monocytogenes infection . Induction of TCM CD4 cells has also been correlated with prolonged survival, thereby highlighting the importance of gaining a better understanding of the mechanisms underlying central memory induction and persistence for successful vaccine development.
In hosts vaccinated with live Listeria-based vaccine, an effective CD8 T cell response is evoked along with generation of sterilizing immunity [70, 71]. On the contrary, the CD8 T cell response to heat killed Listeria monocytogenes (HKLM) vaccination does not elicit protective immunity. Interestingly, though HKLM vaccination fails to confer protective immunity, irradiated Listeria monocytogenes (IRLM) immunization was successful in protecting mice from secondary infection . However, IRL immunization conferred an inferior protection in comparison to live bacterial infection. Whereas the immunological basis for generation of distinct responses to these three forms of same bacterium remains obscure, Khanna et al. propose that the three forms undergo three different transcriptional and translational programs .
Prime-boost vaccination remains the most effective method of choice for inducing higher number of memory T cells combined with increased resistance . However, the classical prime-boost approach requires lengthy time periods between priming and boosting. If the time interval between priming and boosting is shortened, the generated memory cells are downsized to a level below the protective value. Pham et al. using Listeria monocytogenes as a model system devised an alternative cross-priming strategy in the absence of adjuvant to shorten the interval between initial priming and booster immunization . It led to the generation of antigen-specific CD8 T cells with augmented memory function which can be amplified with each passing day to achieve protective levels within a very short time. Ansari et al. evaluated the protective efficacy of Listeria monocytogenes secretory proteins entrapped in archaeosome (liposome made of Archaea derived lipids) and found that the formulation could generate protective memory in the form of TCM and TEM against Listeria monocytogenes infection .
In the last few decades, study of immune response particularly CD8 T cell response to Listeria monocytogenes in mouse model has proved to be instrumental for better understanding of intracellular pathogen induced infections. Understanding CD8 T cell memory generation to Listeria monocytogenes infection is the focus of numerous research groups across the globe owing to the ray of hope it kindles for designing improved vaccines against a gamut of similar infections. As new cells, receptors, adaptors, and regulatory molecules are discovered each day, Listeria monocytogenes is used as a model to decipher their contributions in various host responses including T cell memory generation and till date though it has yielded considerable information on this issue, but the T cell memory picture yet remains petite and requires further studies to get transformed to a comprehensive one.
- L. Travier, S. Guadagnini, E. Gouin, A. Dufour, V. Chenal-Francisque, and P. Cossart, “ActA promotes Listeria monocytogenes aggregation, intestinal colonization and carriage,” PLoS Pathogens, vol. 9, no. 1, Article ID e1003131, 2013.
- M. A. Ansari, S. Zubair, S. Tufail, et al., “Ether lipid vesicle-based antigens impart protection against experimental listeriosis,” International Journal of Nanomedicine, vol. 7, pp. 2433–2447, 2012.
- S. K. B. Cassidy, J. A. Hagar, T. D. Kanneganti, L. Franchi, G. Nuñez, and M. X. D. O'Riordan, “Membrane damage during Listeria monocytogenes infection triggers a caspase-7 dependent cytoprotective response,” PLoS Pathogens, vol. 8, no. 7, Article ID e1002628, 2012.
- M. Farazuddin, M. Alam, A. A. Khan et al., “Efficacy of amoxicillin bearing microsphere formulation in treatment of Listeria monocytogenes infection in Swiss albino mice,” Journal of Drug Targeting, vol. 18, no. 1, pp. 45–52, 2010.
- J. H. Rowe, J. M. Ertelt, L. Xin, and S. S. Way, “Listeria monocytogenes cytoplasmic entry induces fetal wastage by disrupting maternal Foxp3+ regulatory T cell-sustained fetal tolerance,” PLoS Pathogens, vol. 8, no. 8, Article ID e1002873, 2012.
- M. Lara-Tejero and E. G. Pamer, “T cell responses to Listeria monocytogenes,” Current Opinion in Microbiology, vol. 7, no. 1, pp. 45–50, 2004.
- M. Farazuddin, A. Chauhan, R. M. M. Khan, and M. Owais, “Amoxicillin-bearing microparticles: potential in the treatment of Listeria monocytogenes infection in Swiss albino mice,” Bioscience Reports, vol. 31, no. 4, pp. 265–272, 2011.
- S. A. Condotta, M. J. Richer, V. P. Badovinac, and J. T. Harty, “Probing CD8 T cell responses with Listeria monocytogenes infection,” Advances in Immunology, vol. 113, pp. 51–80, 2012.
- M. F. Bachmann, P. Wolint, K. Schwarz, and A. Oxenius, “Recall proliferation potential of memory CD8+ T cells and antiviral protection,” The Journal of Immunology, vol. 175, no. 7, pp. 4677–4685, 2005.
- E. J. Wherry, V. Teichgräber, T. C. Becker et al., “Lineage relationship and protective immunity of memory CD8 T cell subsets,” Nature Immunology, vol. 4, no. 3, pp. 225–234, 2003.
- L. S. Cauley, T. Cookenham, T. B. Miller et al., “Cutting edge: virus-specific CD4+ memory T cells in nonlymphoid tissues express a highly activated phenotype,” The Journal of Immunology, vol. 169, no. 12, pp. 6655–6658, 2002.
- D. Masopust, V. Vezys, E. J. Usherwood et al., “Activated primary and memory CD8 T cells migrate to nonlymphoid tissues regardless of site of activation or tissue of origin,” The Journal of Immunology, vol. 172, no. 8, pp. 4875–4882, 2004.
- K. M. Huster, C. Stemberger, G. Gasteiger, W. Kastenmüller, I. Drexler, and D. H. Busch, “Cutting edge: memory CD8 T cell compartment grows in size with immunological experience but nevertheless can lose function,” The Journal of Immunology, vol. 183, no. 11, pp. 6898–6902, 2009.
- J. J. Obar, E. R. Jellison, B. S. Sheridan et al., “Pathogen-induced inflammatory environment controls effector and memory CD8+ T cell differentiation,” The Journal of Immunology, vol. 187, no. 10, pp. 4967–4978, 2011.
- P. Cossart, “Molecular and cellular basis of the infection by Listeria monocytogenes: an overview,” International Journal of Medical Microbiology, vol. 291, no. 6-7, pp. 401–409, 2002.
- E. Teixeiro, M. A. Daniels, S. E. Hamilton et al., “Different T cell receptor signals determine CD8+ memory versus effector development,” Science, vol. 323, no. 5913, pp. 502–505, 2009.
- S. M. Kaech, S. Hemby, E. Kersh, and R. Ahmed, “Molecular and functional profiling of memory CD8 T cell differentiation,” Cell, vol. 111, no. 6, pp. 837–851, 2002.
- J. T. Chang, V. R. Palanivel, I. Kinjyo et al., “Asymmetric T lymphocyte division in the initiation of adaptive immune responses,” Science, vol. 315, no. 5819, pp. 1687–1691, 2007.
- K. M. Huster, M. Koffler, C. Stemberger, M. Schiemann, H. Wagner, and D. H. Busch, “Unidirectional development of CD8+ central memory T cells into protective Listeria-specific effector memory T cells,” European Journal of Immunology, vol. 36, no. 6, pp. 1453–1464, 2006.
- E. G. Pamer, “Immune responses to Listeria monocytogenes,” Nature Reviews Immunology, vol. 4, no. 10, pp. 812–823, 2004.
- D. Zehn, S. Y. Lee, and M. J. Bevan, “Complete but curtailed T-cell response to very low-affinity antigen,” Nature, vol. 458, no. 7235, pp. 211–214, 2009.
- P. Wong, M. Lara-Tejero, A. Ploss, I. Leiner, and E. G. Pamer, “Rapid development of T cell memory,” The Journal of Immunology, vol. 172, no. 12, pp. 7239–7245, 2004.
- K. M. Kerksiek, A. Ploss, I. Leiner, D. H. Busch, and E. G. Pamer, “H2-M3-restricted memory T cells: persistence and activation without expansion,” The Journal of Immunology, vol. 170, no. 4, pp. 1862–1869, 2003.
- K. M. Huster, V. Busch, M. Schiemann et al., “Selective expression of IL-7 receptor on memory T cells identifies early CD40L-dependent generation of distinct CD8+ memory T cell subsets,” Proceedings of the National Academy of Sciences of the United States of America, vol. 101, no. 15, pp. 5610–5615, 2004.
- M. A. Williams and M. J. Bevan, “Shortening the infectious period does not alter expansion of CD8 T cells but diminishes their capacity to differentiate into memory cells,” The Journal of Immunology, vol. 173, no. 11, pp. 6694–6702, 2004.
- V. P. Badovinac, K. A. N. Messingham, S. E. Hamilton, and J. T. Harty, “Regulation of CD8+ T cells undergoing primary and secondary responses to infection in the same host,” The Journal of Immunology, vol. 170, no. 10, pp. 4933–4942, 2003.
- V. P. Badovinac and J. T. Harty, “Programming, demarcating, and manipulating CD8+ T-cell memory,” Immunological Reviews, vol. 211, pp. 67–80, 2006.
- S. M. Kaech, E. J. Wherry, and R. Ahmed, “Effector and memory T-cell differentiation: implications for vaccine development,” Nature Reviews Immunology, vol. 2, no. 4, pp. 251–262, 2002.
- N.-L. L. Pham, L. L. Pewe, C. J. Fleenor et al., “Exploiting cross-priming to generate protective CD8 T-cell immunity rapidly,” Proceedings of the National Academy of Sciences of the United States of America, vol. 107, no. 27, pp. 12198–12203, 2010.
- E. M. Janssen, N. M. Droin, E. E. Lemmens et al., “CD4+ T-cell help controls CD8+ T-cell memory via TRAIL-mediated activation-induced cell death,” Nature, vol. 434, no. 7029, pp. 88–93, 2005.
- M. A. Williams, B. J. Holmes, J. C. Sun, and M. J. Bevan, “Developing and maintaining protective CD8+ memory T cells,” Immunological Reviews, vol. 211, pp. 146–153, 2006.
- M. A. Williams, A. J. Tyznik, and M. J. Bevan, “Interleukin-2 signals during priming are required for secondary expansion of CD8+ memory T cells,” Nature, vol. 441, no. 7095, pp. 890–893, 2006.
- Z. Xiao, K. A. Casey, S. C. Jameson, J. M. Curtsinger, and M. F. Mescher, “Programming for CD8 T cell memory development requires IL-12 or type I IFN,” The Journal of Immunology, vol. 182, no. 5, pp. 2786–2794, 2009.
- A. M. Intlekofer, N. Takemoto, C. Kao et al., “Requirement for T-bet in the aberrant differentiation of unhelped memory CD8+ T cells,” Journal of Experimental Medicine, vol. 204, no. 9, pp. 2015–2021, 2007.
- N. S. Joshi, W. Cui, A. Chandele et al., “Inflammation directs memory precursor and short-lived effector CD8+ T cell fates via the graded expression of T-bet transcription factor,” Immunity, vol. 27, no. 2, pp. 281–295, 2007.
- D.-M. Zhao, S. Yu, X. Zhou et al., “Constitutive activation of Wnt signaling favors generation of memory CD8 T cells,” The Journal of Immunology, vol. 184, no. 3, pp. 1191–1199, 2010.
- X. Zhou and H.-H. Xue, “Cutting edge: generation of memory precursors and functional memory CD8+ T cells depends on T cell factor-1 and lymphoid enhancer-binding factor-1,” The Journal of Immunology, vol. 189, no. 6, pp. 2722–2726, 2012.
- C. J. Henry, J. M. Grayson, K. L. Brzoza-Lewis et al., “The roles of IL-12 and IL-23 in CD8+ T cell-mediated immunity against Listeria monocytogenes: insights from a DC vaccination model,” Cellular Immunology, vol. 264, no. 1, pp. 23–31, 2010.
- M. M. Sandau, J. E. Kohlmeier, D. L. Woodland, and S. C. Jameson, “IL-15 regulates both quantitative and qualitative features of the memory CD8 T cell pool,” The Journal of Immunology, vol. 184, no. 1, pp. 35–44, 2010.
- P. S. Biswas, V. Pedicord, A. Ploss, E. Menet, I. Leiner, and E. G. Pamer, “Pathogen-specific CD8 T cell responses are directly inhibited by IL-10,” The Journal of Immunology, vol. 179, no. 7, pp. 4520–4528, 2007.
- J. S. Haring and J. T. Harty, “Interleukin-18-related genes are induced during the contraction phase but do not play major roles in regulating the dynamics or function of the T-cell response to Listeria monocytogenes infection,” Infection and Immunity, vol. 77, no. 5, pp. 1894–1903, 2009.
- E. Y. Zhang, B. L. Parker, and T. M. Yankee, “Gads regulates the expansion phase of CD8+ T cell-mediated immunity,” The Journal of Immunology, vol. 186, no. 8, pp. 4579–4589, 2011.
- E. L. Pearce, M. C. Walsh, P. J. Cejas et al., “Enhancing CD8 T-cell memory by modulating fatty acid metabolism,” Nature, vol. 460, no. 7251, pp. 103–107, 2009.
- E. E. Vomhof-DeKrey, J. S. Haring, and G. P. Dorsam, “Vasoactive intestinal peptide receptor 1 is downregulated during expansion of antigen-specific CD8 T cells following primary and secondary Listeria monocytogenes infections,” Journal of Neuroimmunology, vol. 234, no. 1-2, pp. 40–48, 2011.
- R. Dudani, M. Russell, H. van Faassen, L. Krishnan, and S. Sad, “Mutation in the Fas pathway impairs CD8+ T cell memory,” The Journal of Immunology, vol. 180, no. 5, pp. 2933–2941, 2008.
- A. Singh, A. Jatzek, E. H. Plisch, R. Srinivasan, J. Svaren, and M. Suresh, “Regulation of memory CD8 T-cell differentiation by cyclin-dependent kinase inhibitor ,” Molecular and Cellular Biology, vol. 30, no. 21, pp. 5145–5159, 2010.
- J. M. Grayson, A. J. Zajac, J. D. Altman, and R. Ahmed, “Cutting edge: increased expression of Bcl-2 in antigen-specific memory CD8+ T cells,” The Journal of Immunology, vol. 164, no. 8, pp. 3950–3954, 2000.
- I. Dzhagalov, A. Dunkle, and Y.-W. He, “The anti-apoptotic BCL-2 family member Mcl-1 promotes T lymphocyte survival at multiple stages,” The Journal of Immunology, vol. 181, no. 1, pp. 521–528, 2008.
- A. Dunkle, I. Dzhagalov, C. Gordy, and Y.-W. He, “Transfer of CD8+ T cell memory using Bcl-2 as a marker,” The Journal of Immunology, vol. 190, pp. 940–947, 2013.
- J. R. DiSpirito and H. Shen, “Histone acetylation at the single-cell level: a marker of memory CD8+ T cell differentiation and functionality,” The Journal of Immunology, vol. 184, no. 9, pp. 4631–4636, 2010.
- P. Tamás, S. A. Hawley, R. G. Clarke et al., “Regulation of the energy sensor AMP-activated protein kinase by antigen receptor and Ca2+ in T lymphocytes,” Journal of Experimental Medicine, vol. 203, no. 7, pp. 1665–1670, 2006.
- D. G. Hardie, F. A. Ross, and S. A. Hawley, “AMPK: a nutrient and energy sensor that maintains energy homeostasis,” Nature Reviews Molecular Cell Biology, vol. 13, no. 4, pp. 251–262, 2012.
- J. Rolf, M. Zarrouk, D. K. Finlay, M. Foretz, B. Viollet, and D. A. Cantrell, “AMPK1: a glucose sensor that controls CD8 T-cell memory,” European Journal of Immunology, vol. 43, no. 4, pp. 889–896, 2013.
- M. Kursar, K. Bonhagen, A. Köhler, T. Kamradt, S. H. E. Kaufmann, and H.-W. Mittrücker, “Organ-specific CD4+ T cell response during Listeria monocytogenes infection,” The Journal of Immunology, vol. 168, no. 12, pp. 6382–6387, 2002.
- V. P. Badovinac, K. A. N. Messingham, T. S. Griffith, and J. T. Harty, “TRAIL deficiency delays, but does not prevent, erosion in the quality of “helpless” memory CD8 T cells,” The Journal of Immunology, vol. 177, no. 2, pp. 999–1006, 2006.
- J. K. Northrop, R. M. Thomas, A. D. Wells, and H. Shen, “Epigenetic remodeling of the IL-2 and IFN-γ loci in memory CD8 T cells is influenced by CD4 T cells,” The Journal of Immunology, vol. 177, no. 2, pp. 1062–1069, 2006.
- J. A. Sacks and M. J. Bevan, “TRAIL deficiency does not rescue impaired CD8+ T cell memory generated in the absence of CD4+ T cell help,” The Journal of Immunology, vol. 180, no. 7, pp. 4570–4576, 2008.
- J. C. Sun, M. A. Williams, and M. J. Bevan, “CD4+ T cells are required for the maintenance, not programming, of memory CD8+ T cells after acute infection,” Nature Immunology, vol. 5, no. 9, pp. 927–933, 2004.
- M. Kursar, K. Bonhagen, J. Fensterle et al., “Regulatory CD4+CD25+ T cells restrict memory CD8+ T cell responses,” Journal of Experimental Medicine, vol. 196, no. 12, pp. 1585–1592, 2002.
- M. Kursar, A. Köhler, S. H. E. Kaufmann, and H.-W. Mittrücker, “Depletion of CD4+ T cells during immunization with nonviable Listeria monocytogenes causes enhanced CD8+ T cell-mediated protection against listeriosis,” The Journal of Immunology, vol. 172, no. 5, pp. 3167–3172, 2004.
- L. Pace, A. Tempez, C. Arnold-Schrauf, F. Lemaitre, P. Bousso, and L. Fetler, “Regulatory T cells increase the avidity of primary CD8+ T cell responses and promote memory,” Science, vol. 338, no. 6106, pp. 532–536, 2012.
- C. Bourgeois, B. Rocha, and C. Tanchot, “A role for CD40 expression on CD8+ T cells in the generation of CD8+ T cell memory,” Science, vol. 297, no. 5589, pp. 2060–2063, 2002.
- E. M. Janssen, E. E. Lemmens, T. Wolfe, U. Christen, M. G. von Herrath, and S. P. Schoenberger, “CD4+ T cells are required for secondary expansion and memory in CD8+ T lymphocytes,” Nature, vol. 421, no. 6925, pp. 852–856, 2003.
- L. E. Edwards, C. Haluszczak, and R. M. Kedl, “Phenotype and function of protective, CD4-independent CD8 T cell memory,” Immunologic Research, vol. 55, no. 1–3, pp. 135–145, 2013.
- H. Shen, J. K. Whitmire, X. Fan, D. J. Shedlock, S. M. Kaech, and R. Ahmed, “A specific role for B cells in the generation of CD8 T cell memory by recombinant Listeria monocytogenes,” The Journal of Immunology, vol. 170, no. 3, pp. 1443–1451, 2003.
- D. Gray, “Immunological memory,” Annual Review of Immunology, vol. 11, pp. 49–77, 1993.
- M. S. Asano and R. Ahmed, “CD8 T cell memory in B cell-deficient mice,” Journal of Experimental Medicine, vol. 183, no. 5, pp. 2165–2174, 1996.
- F. Di Rosa and P. Matzinger, “Long-lasting CD8 T cell memory in the absence of CD4 T cells or B cells,” Journal of Experimental Medicine, vol. 183, no. 5, pp. 2153–2163, 1996.
- M.-A. Bründler, P. Aichcle, M. Bachmann, D. Kitamura, K. Rajewsky, and R. M. Zinkernagel, “Immunity to viruses in B cell-deficient mice: influence of antibodies on virus persistence and on T cell memory,” European Journal of Immunology, vol. 26, no. 9, pp. 2257–2262, 1996.
- L. Lefrançois, A. Marzo, and K. Williams, “Sustained response initiation is required for T cell clonal expansion but not for effector or memory development in vivo,” The Journal of Immunology, vol. 171, no. 6, pp. 2832–2839, 2003.
- K. M. Khanna, D. A. Blair, A. T. Vella, S. J. McSorley, S. K. Datta, and L. Lefrançois, “T cell and APC dynamics in situ control the outcome of vaccination,” The Journal of Immunology, vol. 185, no. 1, pp. 239–252, 2010.