Circulating CD3+CD4+CD161+ Cells Are Associated with Early Complications after Autologous Stem Cell Transplantation in Multiple Myeloma

Lee, Sung-Eun; Lim, Ji-Young; Ryu, Da-Bin; Kim, Tae Woo; Jeon, Young-Woo; Yoon, Jae-Ho; Cho, Byung-Sik; Eom, Ki-Seong; Kim, Yoo-Jin; Kim, Hee-Je; Lee, Seok; Cho, Seok-Goo; Kim, Dong-Wook; Lee, Jong Wook; Min, Woo-Sung; Min, Chang-Ki

doi:https://doi.org/10.1155/2018/5097325

BioMed Research International

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Abstract Introduction Materials and Methods Results Discussion Conclusions Conflicts of Interest Acknowledgments Supplementary Materials References Copyright Related Articles

Research Article | Open Access

Volume 2018 | Article ID 5097325 | https://doi.org/10.1155/2018/5097325

Circulating CD3⁺CD4⁺CD161⁺ Cells Are Associated with Early Complications after Autologous Stem Cell Transplantation in Multiple Myeloma

Sung-Eun Lee,¹Ji-Young Lim,¹Da-Bin Ryu,¹Tae Woo Kim,¹Young-Woo Jeon,¹Jae-Ho Yoon,¹Byung-Sik Cho,^1,2Ki-Seong Eom,^1,2Yoo-Jin Kim,^1,2Hee-Je Kim,^1,2Seok Lee,^1,2and Seok-Goo Cho¹ et al.

Academic Editor: Roberto Crocchiolo

Received11 Jul 2017

Revised14 Sept 2017

Accepted04 Dec 2017

Published01 Jan 2018

Abstract

The aim of this study was to explore if measurement of pretransplant circulating CD161-expressing cells, in addition to clinical risk factors, could predict mucositis and infections in patients with multiple myeloma (MM) undergoing autologous stem cell transplantation (ASCT). To determine if CD161-expressing cells are likely to predict early complications, namely, mucositis (≥grade 3), infections, and cytomegalovirus (CMV) reactivation, we prospectively examined CD161-expressing cells (CD3⁺CD4⁺CD161⁺ and CD3⁺CD8⁺CD161⁺) in peripheral blood samples from 108 patients with MM undergoing ASCT. After adjusting for factors identified by univariate analysis that predicted mucositis (≥grade 3), infection before engraftment, and CMV reactivation, multivariate analyses revealed that the low proportion of CD3⁺CD4⁺CD161⁺ cells in peripheral blood was an independent predictor of mucositis (≥grade 3) (), infections before engraftment (), and CMV reactivation (). In addition, we found that female sex and decreased glomerular filtration rate were independent factors for predicting mucositis. Female sex and severe pulmonary comorbidity were independent factors for predicting infection before engraftment. We found that the proportion of circulating CD3⁺CD4⁺CD161⁺ cells is useful for predicting the occurrence of early complications, including mucositis and infections, after ASCT in patients with MM.

1. Introduction

High-dose therapy followed by autologous stem cell transplantation (ASCT) is the standard of care for transplant-eligible patients with multiple myeloma (MM) [1–4]. Although dose intensification of melphalan yields therapeutic effects, this approach also results in treatment-related toxicities such as mucositis and infections, which are the most important causes of treatment-related complications [5, 6]. Infections during the profound neutropenia in the preengraftment phase of transplantation can progress rapidly, leading to other life-threatening complications. Moreover, patients with MM are at high risk of both bacterial and viral infections due to patient- and disease-related factors as well as treatment-related factors [7]. Therefore, it is critical to recognize neutropenic fever early and to promptly initiate empiric systemic antibacterial therapy to avoid mortality.

The innate immune system is a first line of defense against pathogens and sterile injury [8]. Innate immune cells including monocytes, macrophages, neutrophils, NK cells, NKT cells, and γδ cells recognize broadly expressed molecules derived from pathogens or apoptotic cells, and their activation plays an important role in priming adaptive immune responses. Considering that before the initial engraftment a patient’s remaining innate immune system may play defensive roles against infections, we previously evaluated the influence of a circulating innate T cell subtype, CD161-expressing T cells, on early outcomes after allogeneic SCT. In particular, circulating CD3⁺CD4⁺CD161⁺ cell proportion was a risk factor for the occurrence of clinically or microbiologically documented infections before engraftment [9].

Although the influence of CD161-expressing T cells on early complications after allogeneic SCT has been examined [9], their role in early complications after ASCT in patients with MM, who have different medical conditions and immune system characteristics, are uncertain. In this study, we explored the ability of circulating CD161-expressing cells (as detected prior to ASCT) to predict mucositis and infections in patients with MM undergoing ASCT. In addition to the immune parameters, we also investigated clinical risk factors that could predict patient outcomes.

2. Materials and Methods

2.1. Patient Selection

A total of 108 consecutive patients with MM who underwent ASCT as part of front-line treatment at our institution between January 2012 and December 2015 were included in this analysis. To identify novel immune cell biomarkers predictive of early complications, we prospectively obtained peripheral blood samples before they underwent conditioning chemotherapy. In addition, various clinical and laboratory data that we hypothesized may contribute to the early development of complications following ASCT collected before the conditioning regimen was initiated. All patients received a pulmonary function test, echocardiography, liver Doppler ultrasound, and infection assessment prior to ASCT. The Institutional Review Board of the Catholic University of Korea approved the research protocol for all data analysis. This study was also conducted in accordance with the Declaration of Helsinki.

2.2. Transplant Procedures

ASCT was performed after achieving a response greater than a partial response (PR). Some patients without progressive MM who were resistant to various agents (bortezomib and thalidomide) underwent ASCT. General ASCT procedures were performed as described previously [10, 11]. Briefly, all patients were mobilized with cyclophosphamide (3 g/m² total) for 2 days and then treated subcutaneously once daily with G-CSF (lenograstim, JW Pharmaceutical, Seoul, Korea) at 10 μg/kg/day. Conditioning consisted of melphalan (100 mg/m²) for 2 days except in patients with serum creatinine above 2.0 mg/dl or on hemodialysis, for whom 70 mg/m² for 2 days was used. G-CSF (5 μg/kg/day) was given subcutaneously to all patients from one day after transplantation until the absolute neutrophil count (ANC) reached >3.0 × 10⁹/L. All patients received prophylactic ciprofloxacin and an antifungal agent (micafungin) starting 4 days before transplantation and continued to receive these drugs until the ANC reached 1.5 × 10⁹/L.

2.3. Isolation of Mononuclear Cells and Flow Cytometric Analysis

Blood samples for cell population analysis were collected one day before conditioning chemotherapy. Peripheral blood mononuclear cells (PBMCs) were isolated from whole blood samples (10 mL) collected in EDTA-coated tubes by centrifugation in Ficoll-Paque Plus. PBMCs were processed immediately for analysis. Flow cytometry was used to evaluate the percentages of CD3⁺, CD4⁺CD161⁺, and CD8⁺CD161⁺ T cells; natural killer (NK) cells (CD16⁺CD56⁺); and myeloid-derived suppressor cells (MDSCs) [Lin^-HLA-DR^-CD11b⁺CD33⁺ (granulocytic) and HLA-DR^-CD14⁺ (monocytic)]. Anti-CD3-allophycocyanin (APC), anti-CD4-fluorescein isothiocyanate (FITC), anti-CD8-phycoerythrin (PE), anti-CD161-PerCP-Cy5.5, anti-CD16-FITC, anti-CD56-PE, and anti-CD14-APC monoclonal antibodies (mAbs) were purchased from eBioscience (San Diego, CA, USA). Anti-Lineage cocktail 1 (Lin 1)-FITC, anti-HLA-DR-PerCP, rat anti-mouse CD11b-APC-Cy™7, and mouse anti-human CD33-V450 (BD BioSciences) mAbs were purchased from BD Biosciences (San Jose, CA). CD4⁺CD161⁺ and CD8⁺CD161⁺ T cells were gated on CD3⁺ cells and are expressed as percentages of lymphocytes. The frequencies of HLA-DR^-Lin^-CD11b⁺CD33⁺ and HLA-DR^-CD14⁺ MDSCs are expressed as percentages of total PBMCs. Flow cytometry was performed using a FACS LSR Fortessa (BD Biosciences).

2.4. Definitions

Toxicity was classified using the National Cancer Institute Common Toxicity Criteria grading scheme. Infections included microbially and clinically defined infections as proposed by the Immunocompromised Host Society [12, 13], and in this study, fevers of unknown origin were excluded. For surveillance of cytomegalovirus (CMV) reactivation, quantitative real-time PCR (qPCR) for CMV DNA after neutrophil engraftment was tested using a LightCycler® 2.0 instrument (Roche Diagnostics, Mannheim, Germany). CMV reactivation was diagnosed when a patient previously found to be CMV seropositive exhibited >500 copies/mL by qPCR. Early clinical complications assessed were mucositis (≥grade 3), infection before engraftment, and CMV reactivation after engraftment. Severity of comorbidities was classified using definitions from the hematopoietic cell transplantation-specific comorbidity index [14].

2.5. Statistical Analysis

Potential risk factors for the occurrence of early complications in patients with MM undergoing ASCT were assessed using logistic regression analysis. Optimal cutoffs for continuous variables were identified using receiver operating characteristic (ROC) curve analysis. To investigate whether the identified markers were independent predictors, covariates with a value less than 0.1 in the univariate analyses were added to the multivariate analysis model. Student’s -test was used to compare continuous variables.

3. Results

3.1. Patient Characteristics and Early Complications

A total of 108 patients with MM were analyzed, of whom 64 (59%) were male and 44 (41%) were female. The median age was 56 years (range, 32–67 years) and the median disease duration before ASCT was 6.8 months (range, 2.9–21.6 months). Demographic information for all patients is listed in Table 1.

Among the 108 patients, 54 patients (50%) developed mucositis, including 25 with grade 2 and 29 with ≥grade 3. Analysis of risk factors was performed for mucositis (≥grade 3), because mucositis (≥grade 3) had a substantial effect on infection risk. The incidence of infection before engraftment was 52%. Twenty-nine patients (27%) developed CMV reactivation, nine of whom received ganciclovir therapy. One patient died due to severe sepsis within 100 days.

3.2. Analysis of CD161⁺ T Cell Count prior to ASCT

The median MNC count was 1.2 × 10⁶ cells/mL (range, 0.2–3.4 × 10⁶ cells/mL), and the mean (±standard error) proportions of CD3⁺CD4⁺CD161⁺ T cells and CD3⁺CD8⁺CD161⁺ T cells were % and %, respectively. The proportions of CD3⁺CD4⁺CD161⁺ and CD3⁺CD8⁺CD161⁺ T cells were compared according to the occurrence of mucositis (≥grade 3), infection before engraftment, and CMV reactivation (Figure 1). The proportion of CD3⁺CD4⁺CD161⁺ T cells was lower in patients who developed infection before engraftment (% versus %, ) and CMV reactivation (% versus %, ). Patients with mucositis ≥ grade 3 tended to have a lower proportion of CD3⁺CD4⁺CD161⁺ T cells (% versus %, ). In contrast, the proportion of CD3⁺CD8⁺CD161⁺ T cells was not associated with early complications.

(a)

(b)

(c)

In addition, although we compared the proportions of NK cells and MDSCs according to the occurrence of mucositis (≥grade 3), infection before engraftment, and CMV reactivation in 59 patients with available data, there were no significant associations with early complications (Supplementary Table 1).

3.3. Risk Factors for Mucositis (≥Grade 3)

The results of univariate analysis for potential risk factors predicting the development of mucositis (≥grade 3) following ASCT are listed in Table 2. To explicitly assess renal comorbid condition in patients with MM, both serum creatinine and glomerular filtration rate (GFR), which was calculated using the modification of diet in renal disease (MDRD), were included as continuous variables. Decreased proportion of CD3⁺CD4⁺CD161⁺ T cells was associated with the occurrence of mucositis (≥grade 3). Female sex, decreased body mass index (BMI), and decreased GFR were also factors that predicted the occurrence of mucositis (≥grade 3).

In multivariate analysis (Table 3), stratification of patients into low and high groups based on the proportion of CD3⁺CD4⁺CD161⁺ T cells by ROC curve analysis revealed a significant protective role for the proportion of pretransplant CD3⁺CD4⁺CD161⁺ cells against the occurrence of mucositis (≥grade 3) (cutoff of 3.72%, relative risk (RR) of 0.19, ). In addition, female sex () and decreased GFR () were independent risk factors. Patients with decreased BMI tended to have a higher mucositis rate () (Figure 2(a)).

(a)

(b)

3.4. Risk Factors for Infection before Engraftment and CMV Reactivation

Female sex, decreased BMI, decreased GFR, and severe pulmonary comorbidity predicted the occurrence of infection before engraftment. In addition, decreased BMI predicted the occurrence of CMV reactivation (Table 2). These clinical factors were included in multivariate analysis (Table 3). The low proportion of CD3⁺CD4⁺CD161⁺ T cells was significantly associated with a higher risk of infection before engraftment (cutoff of 3.72%, RR of 0.20, and ) and CMV reactivation (cutoff of 3.72%, RR of 0.25, and ). In addition, female sex and severe pulmonary comorbidity were associated with the occurrence of infection before engraftment ( and , resp.) (Figure 2(b)).

4. Discussion

Myeloablative high-dose chemotherapy followed by ASCT prolongs survival for patients with MM [1, 2, 15, 16]. Although the value of high-dose chemotherapy has been debated for years because of a meta-analysis that showed no clear overall survival benefit [17], ASCT as a first-line treatment is still the standard of care, and novel agents have markedly improved response depth before and after ASCT [18–21]. However, because of the toxic effects of ASCT and the advanced age of many patients with MM, accurate assessment of eligibility is crucial [22]. Moreover, in addition to the toxicities associated with ASCT, patients with MM are susceptible to infection [23] due to dysfunctions in humoral immunity and various immune system including T cells [24–26], dendritic cells [27], and natural killer cells [28]. In addition, the preengraftment period is particularly important in ASCT because the rapid reconstitution of humoral and cellular immunity results in a reduced risk of opportunistic infection by 3 months after ASCT. Therefore, we focused on patient and transplant characteristics that we thought might be important for predicting early complications in patients with MM undergoing ASCT. In particular, we explored the influence of circulating CD161-expressing T cell populations as measured prior to ASCT on early complications based on the reason that, before the initial engraftment, the patient’s remaining immune system may defend against mucositis and subsequent infections, particularly during profound neutropenia.

CD161 is a type II transmembrane glycoprotein with characteristics of the C-type lectin superfamily. This receptor is expressed on NK cells, 25% of all adult peripheral T cells, more than 90% of all peripheral blood monocytes, and on in vitro-derived dendritic cells [29]. We previously evaluated the association of CD161-expressing T cells with the development of acute graft-versus-host disease after allogeneic SCT and found that a low proportion of CD8⁺CD161⁺ cells and a high ratio of CD4⁺CD161⁺ cells to CD8⁺CD161⁺ cells from peripheral blood at engraftment were associated with the occurrence of acute graft-versus-host disease, with evidence of higher expression of the Th17 transcription factor RORγT in CD4⁺CD161⁺ T cells rather than CD8⁺CD161⁺ T cells [30]. Furthermore, we reported that in 282 patients receiving allogeneic SCT pretransplant circulating CD3⁺CD4⁺CD161⁺ cell proportion was associated with the occurrence of neutropenic infections, suggesting the importance of CD3⁺CD4⁺CD161⁺ cells in a rapid immune response to microorganisms before establishment of the posttransplant immune system [9]. In the present study, we showed that pretransplant proportion of CD3⁺CD4⁺CD161⁺ T cells in patients with MM undergoing ASCT can predict the occurrence of early complications, suggesting that CD161-expressing T cells play an important role in the inflammatory milieu.

In this study, we sought to identify predictors of mucositis in a homogeneous group of patients with MM undergoing ASCT following high-dose melphalan treatment, because mucositis risk is believed to vary according to the conditioning regimen intensity, SCT type (autologous versus allogeneic), and patient-related factors. Regarding SCT-associated mucositis, previous studies have reported that significant oral mucositis occurs in about 75% of all patients undergoing SCT [31–33] according to the type of chemotherapeutic agent, with high-dose melphalan known to cause severe mucositis [32]. Importantly, severe mucositis not only extends hospitalization and increases cost, but also may be associated with increased mortality. Rapoport et al. showed that severe mucositis was correlated with increased incidences of bacteremia and mortality [34]. In their study, 60% of all patients with a peak mucositis score of 18 or higher according to the Oral Assessment Guide (OAG) [35] developed bacteremia, compared with 30% of all patients with peak scores lower than 18 (). Additionally, an association between infection and severe mucositis was supported by a study that reported that streptococcal infections were three times more prevalent in patients with severe ulcerative mucositis than patients with mild symptoms [36]. In this study, we also found a substantial effect of severe mucositis on infection risk during the preengraftment period (data not shown) and identified a significant protective role for pretransplant CD3⁺CD4⁺CD161⁺ T cells against the occurrence of mucositis (≥grade 3), in addition to clinical factors including female sex and decreased GFR. Using biomarkers as predictors of early complications in ASCT, we can assess transplant eligibility and identify those patients most likely to benefit from dose modification of conditioning chemotherapy and additional prophylactic treatments. Although the clinical predictors found in our study can also help establish treatment strategies to reduce excessive transplant toxicities, obviously we have several limitations of the small size of patient population and missed risk factors.

CMV reactivation has been demonstrated to be relatively common after ASCT for MM (48.5%), especially when tandem transplantation is performed using combination chemotherapy with high-dose melphalan [37]. We observed CMV reactivation in approximately 27% of all patients and found that the proportion of pretransplant CD3⁺CD4⁺CD161⁺ T cells was lower in patients with CMV reactivation than those without CMV reactivation. Kang et al. analyzed CD161 expression and cytokine secretion in CD4⁺ T cells in blood and liver samples from patients infected with hepatitis C. They observed marked enrichment of CD161⁺CD4⁺ T cells in the liver during chronic hepatitis and a population of CD4⁺ T cells cosecreting IL-22 and IFN-γ [38]. Therefore, further studies are required to characterize the phenotypes of these cells and to assess their immunological functions in viral inflammation.

5. Conclusions

We identified that circulating CD3⁺CD4⁺CD161⁺ T cells, in addition to clinical risk factors, were associated with the occurrence of early complications in the setting of ASCT in patients with MM. Pretransplant predictive immune markers that can predict the occurrence of early complications will help assess transplant eligibility and identify those patients who require dose modification of conditioning chemotherapy and intensified prophylactic strategies.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Acknowledgments

This research was supported by a grant from the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry of Health & Welfare, Republic of Korea (no. HI16C0047).

Supplementary Materials

Supplementary Table 1: pretransplant cell populations according to the occurrence of mucositis, infection, and CMV reactivation. (Supplementary Materials)

References

J. A. Child, G. J. Morgan, and F. E. Davies, “High-dose chemotherapy with hematopoietic stem-cell rescue for multiple myeloma,” The New England Journal of Medicine, vol. 348, no. 19, pp. 1875–1883, 2003.
View at: Publisher Site | Google Scholar
A. Palumbo, F. Cavallo, F. Gay et al., “Autologous transplantation and maintenance therapy in multiple myeloma,” The New England Journal of Medicine, vol. 371, no. 10, pp. 895–905, 2014.
View at: Publisher Site | Google Scholar
H. W. Auner, R. Szydlo, J. Hoek et al., “Trends in autologous hematopoietic cell transplantation for multiple myeloma in Europe: Increased use and improved outcomes in elderly patients in recent years,” Bone Marrow Transplantation, vol. 50, no. 2, pp. 209–215, 2015.
View at: Publisher Site | Google Scholar
S. V. Rajkumar, “Multiple myeloma: 2016 update on diagnosis, risk-stratification, and management,” American Journal of Hematology, vol. 91, no. 7, pp. 719–734, 2016.
View at: Publisher Site | Google Scholar
M. Vera-Llonch, G. Oster, C. M. Ford, J. Lu, and S. Sonis, “Oral mucositis and outcomes of autologous hematopoietic stem-cell transplantation following high-dose melphalan conditioning for multiple myeloma,” The Journal of Supportive Oncology, vol. 5, no. 5, pp. 231–235, 2007.
View at: Google Scholar
G. Reich, M. Y. Mapara, P. Reichardt, B. Dörken, and G. Maschmeyer, “Infectious complications after high-dose chemotherapy and autologous stem cell transplantation: Comparison between patients with lymphoma or multiple myeloma and patients with solid tumors,” Bone Marrow Transplantation, vol. 27, no. 5, pp. 525–529, 2001.
View at: Publisher Site | Google Scholar
B. W. Teh, S. J. Harrison, M. Pellegrini, K. A. Thursky, L. J. Worth, and M. A. Slavin, “Changing treatment paradigms for patients with plasma cell myeloma: Impact upon immune determinants of infection,” Blood Reviews, vol. 28, no. 2, pp. 75–86, 2014.
View at: Publisher Site | Google Scholar
J. H. Spahn, W. Li, and D. Kreisel, “Innate immune cells in transplantation,” Current Opinion in Organ Transplantation, vol. 19, no. 1, pp. 14–19, 2014.
View at: Publisher Site | Google Scholar
T. W. Kim, S.-E. Lee, J.-Y. Lim et al., “Clinical significance of pre-transplant circulating CD3+CD4+CD161+ cell frequency on the occurrence of neutropenic infections after allogeneic stem cell transplantation,” Transplant Infectious Disease, vol. 19, no. 1, Article ID e12643, 2017.
View at: Publisher Site | Google Scholar
S.-E. Lee, S.-A. Yahng, B.-S. Cho et al., “Lymphocyte subset analysis for the assessment of treatment-related complications after autologous stem cell transplantation in multiple myeloma,” Cytotherapy, vol. 14, no. 4, pp. 505–512, 2012.
View at: Publisher Site | Google Scholar
S.-E. Lee, J.-H. Yoon, S.-H. Shin et al., “Impact of failed response to novel agent induction in autologous stem cell transplantation for multiple myeloma,” Annals of Hematology, vol. 93, no. 4, pp. 627–634, 2014.
View at: Publisher Site | Google Scholar
C. Straka, M. Sandherr, H. Salwender et al., “Testing G-CSF responsiveness predicts the individual susceptibility to infection and consecutive treatment in recipients of high-dose chemotherapy,” Blood, vol. 117, no. 7, pp. 2121–2128, 2011.
View at: Publisher Site | Google Scholar
P. A. Pizzo, D. Armstrong, G. Bodely et al., “From the immunocompromised host society: The design, analysis, and reporting of clinical trials on the empirical antibiotic management of the neutropenic patient,” The Journal of Infectious Diseases, vol. 161, no. 3, pp. 397–401, 1990.
View at: Publisher Site | Google Scholar
M. L. Sorror, M. B. Maris, and R. Storb, “Hematopoietic cell transplantation (HCT)-specific comorbidity index: a new tool for risk assessment before allogeneic HCT,” Blood, vol. 106, no. 8, pp. 2912–2919, 2005.
View at: Publisher Site | Google Scholar
M. Attal, J.-L. Harousseau, A.-M. Stoppa et al., “A prospective, randomized trial of autologous bone marrow transplantation and chemotherapy in multiple myeloma,” The New England Journal of Medicine, vol. 335, no. 2, pp. 91–97, 1996.
View at: Publisher Site | Google Scholar
S. Giralt, E. A. Stadtmauer, J. L. Harousseau et al., “International myeloma working group (IMWG) consensus statement and guidelines regarding the current status of stem cell collection and high-dose therapy for multiple myeloma and the role of plerixafor (AMD 3100),” Leukemia, vol. 23, no. 10, pp. 1904–1912, 2009.
View at: Publisher Site | Google Scholar
A. Kumar, S. Galeb, and B. Djulbegovic, “Treatment of patients with multiple myeloma: An overview of systematic reviews,” Acta Haematologica, vol. 125, no. 1-2, pp. 8–22, 2010.
View at: Publisher Site | Google Scholar
M. Cavo, P. Tacchetti, F. Patriarca et al., “Bortezomib with thalidomide plus dexamethasone compared with thalidomide plus dexamethasone as induction therapy before, and consolidation therapy after, double autologous stem-cell transplantation in newly diagnosed multiple myeloma: a randomised phase 3 study,” The Lancet, vol. 376, no. 9758, pp. 2075–2085, 2010.
View at: Publisher Site | Google Scholar
P. Moreau, H. Avet-Loiseau, T. Facon et al., “Bortezomib plus dexamethasone versus reduced-dose bortezomib, thalidomide plus dexamethasone as induction treatment before autologous stem cell transplantation in newly diagnosed multiple myeloma,” Blood, vol. 118, no. 22, pp. 5752–5758, 2011.
View at: Publisher Site | Google Scholar
L. Rosinol, A. Oriol, A. I. Teruel et al., “Superiority of bortezomib, thalidomide, and dexamethasone (VTD) as induction pretransplantation therapy in multiple myeloma: a randomized phase 3 PETHEMA/GEM study,” Blood, vol. 120, no. 8, pp. 1589–1596, 2012.
View at: Google Scholar
M. Attal, V. Lauwers-Cances, and G. Marit, “Lenalidomide maintenance after stem-cell transplantation for multiple myeloma,” The New England Journal of Medicine, vol. 366, no. 19, pp. 1782–1791, 2012.
View at: Publisher Site | Google Scholar
J. Koreth, C. S. Cutler, B. Djulbegovic et al., “High-dose therapy with single autologous transplantation versus chemotherapy for newly diagnosed multiple myeloma: a systematic review and meta-analysis of randomized controlled trials,” Biology of Blood and Marrow Transplantation, vol. 13, no. 2, pp. 183–196, 2007.
View at: Publisher Site | Google Scholar
B. W. Teh, S. J. Harrison, L. J. Worth, T. Spelman, K. A. Thursky, and M. A. Slavin, “Risks, severity and timing of infections in patients with multiple myeloma: A longitudinal cohort study in the era of immunomodulatory drug therapy,” British Journal of Haematology, vol. 171, no. 1, pp. 100–108, 2015.
View at: Publisher Site | Google Scholar
K. H. G. Mills and J. C. Cawley, “Abnormal monoclonal antibody‐defined helper/suppressor T‐cell subpopulations in multiple myeloma: relationship to treatment and clinical stage,” British Journal of Haematology, vol. 53, no. 2, pp. 271–275, 1983.
View at: Publisher Site | Google Scholar
H. Ogawara, H. Handa, T. Yamazaki et al., “High Th1/Th2 ratio in patients with multiple myeloma,” Leukemia Research, vol. 29, no. 2, pp. 135–140, 2005.
View at: Publisher Site | Google Scholar
M. Peres-Andres, J. Almeida, M. Martin-Ayuso et al., “Characterization of bone marrow T cells in monoclonal gammopathy of undetermined significance, multiple myeloma, and plasma cell leukemia demonstrates increased infiltration by cytotoxic/Th1 T cells demonstrating a squed TCR-Vβ repertoire,” Cancer, vol. 106, no. 6, pp. 1296–1305, 2006.
View at: Publisher Site | Google Scholar
R. D. Brown, B. Pope, A. Murray et al., “Dendritic cells from patients with myeloma are numerically normal but functionally defective as they fail to up-regulate CD80 (B7-1) expression after huCD40LT stimulation because of inhibition by transforming growth factor-β₁ and interleukin-10,” Blood, vol. 98, no. 10, pp. 2992–2998, 2001.
View at: Publisher Site | Google Scholar
V. Jurisic, T. Srdic, G. Konjevic, O. Markovic, and M. Colovic, “Clinical stage-depending decrease of NK cell activity in multiple myeloma patients,” Medical Oncology, vol. 24, no. 3, pp. 312–317, 2007.
View at: Publisher Site | Google Scholar
E. G. Iliopoulou, M. V. Karamouzis, I. Missitzis et al., “Increased frequency of CD4+ cells expressing CD161 in cancer patients,” Clinical Cancer Research, vol. 12, no. 23, pp. 6901–6909, 2006.
View at: Publisher Site | Google Scholar
S.-E. Lee, J.-Y. Lim, J.-H. Yoon et al., “CD161+ T Cells as Predictive Markers for Acute Graft-versus-Host Disease,” Biology of Blood and Marrow Transplantation, vol. 21, no. 3, pp. 421–428, 2015.
View at: Publisher Site | Google Scholar
S.-B. Woo, S. T. Sonis, M. M. Monopoli, and A. L. Sonis, “A longitudinal study of oral ulcerative mucositis in bone marrow transplant recipients,” Cancer, vol. 72, no. 5, pp. 1612–1617, 1993.
View at: Publisher Site | Google Scholar
J.-L. Pico, A. Avila-Garavito, and P. Naccache, “Mucositis: its occurrence, consequences, and treatment in the oncology setting,” The Oncologist, vol. 3, no. 6, pp. 446–451, 1998.
View at: Google Scholar
S. I. Bearman, F. R. Appelbaum, C. D. Buckner et al., “Regimen-related toxicity in patients undergoing bone marrow transplantation,” Journal of Clinical Oncology, vol. 6, no. 10, pp. 1562–1568, 1988.
View at: Publisher Site | Google Scholar
A. P. Rapoport, L. F. Miller Watelet, T. Linder et al., “Analysis of factors that correlate with mucositis in recipients of autologous and allogeneic stem-cell transplants,” Journal of Clinical Oncology, vol. 17, no. 8, pp. 2446–2453, 1999.
View at: Publisher Site | Google Scholar
J. Eilers, A. M. Berger, and M. C. Petersen, “Development, testing, and application of the oral assessment guide,” Oncol Nurs Forum, vol. 15, no. 3, pp. 325–330, 1988.
View at: Google Scholar
T. J. Ruescher, A. Sodeifi, S. J. Scrivani, L. B. Kaban, and S. T. Sonis, “The impact of mucositis on α-hemolytic streptococcal infection in patients undergoing autologous bone marrow transplantation for hematologic malignancies,” Cancer, vol. 82, no. 11, pp. 2275–2281, 1998.
View at: Publisher Site | Google Scholar
J. H. Kim, C. Goulston, S. Sanders et al., “Cytomegalovirus Reactivation Following Autologous Peripheral Blood Stem Cell Transplantation for Multiple Myeloma in the Era of Novel Chemotherapeutics and Tandem Transplantation,” Biology of Blood and Marrow Transplantation, vol. 18, no. 11, pp. 1753–1758, 2012.
View at: Publisher Site | Google Scholar
Y.-H. Kang, B. Seigel, B. Bengsch et al., “CD161+CD4+ T cells are enriched in the liver during chronic hepatitis and associated with co-secretion of IL-22 and IFN-γ,” Frontiers in Immunology, vol. 3, article 346, 2012.
View at: Publisher Site | Google Scholar

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Copyright © 2018 Sung-Eun Lee 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.

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