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Volume 2012 (2012), Article ID 670579, 7 pages
Possible Influence of Resistance to Malaria in Clinical Presentation of Rheumatoid Arthritis: Biological Significance of Natural Selection
1Division of Rheumatology, Department of Internal Medicine, Fundación Valle del Lili and ICESI University School of Medicine, Cali, Colombia
2Laboratory of Immunorheumatology, Carrera 98 N. 18-49, Cali, Colombia
Received 6 August 2012; Accepted 21 October 2012
Academic Editor: Masami Takei
Copyright © 2012 Fabio Bonilla-Abadía 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.
Rheumatoid arthritis (RA) is a common autoimmune disease that affects all ethnic groups. Genetic factors, mainly HLA alleles, are highly associated with increased risk to develop RA. However, there are few available data about the role of these genetic polymorphisms in the prevalence or severity of RA in the Afrodescendant population, who have evolutionarily and by natural selection developed mutations that allowed them to acquire resistance to infectious diseases like malaria. Some of the mechanisms, by which this resistance was developed as a product of natural selection, are involved in different forms of immunological response, many of them of a well-known importance in the pathophysiology of RA. This paper focuses on presenting the known mechanisms of resistance to malaria and their possible contribution to the pathophysiology of RA, including “loss-of-function” mutations, lack of expression of chemokine receptors, decrease of immune complexes clearance by asplenia, or increase of immune reactivity mediated by B cells, among other mechanisms in this special group of patients.
Rheumatoid arthritis (RA) is a common disease that affects all ethnic groups with a prevalence estimated between 0.5 and 1% of the general population . It is a chronic autoimmune disorder with a systemic character and several clinical variables. Multiple responses are generated by inflammatory cascades mediated by various molecules such as cytokines, adhesion molecules, chemokines, and cells such as lymphocytes T and B lymphocytes, leading to a final common pathway that predominantly affects the joints and structures of the synovial membrane, articular cartilage, and bone [2, 3]. The factors associated with the development of the disease comprise genetic and environmental factors. These include female gender, family history of RA, age, smoking, and genetic factors, including the Human Leukocyte Antigen (HLA) and non-HLA such as polymorphisms of PTPN22, STAT-4, tumor necrosis factor-α (TNF-α), T-cell receptor (TCR), and Fc-γ receptor (Fc-γR), among others. The evidence on genetic susceptibility pointed at RA is mainly obtained from cohorts of Caucasians and Asian patients. Among white individuals who have RA, 80% express HLA-DR1 or HLA-DR4 . However, there are few available data about the role of these genetic polymorphisms in the prevalence or severity of RA in the Afrodescendants (AD), who have evolutionarily and by natural selection developed mutations that allowed them to acquire resistance to infectious diseases like malaria. Some of the mechanisms by which this resistance was developed as a product of natural selection are involved in different forms of immunological pathways, many of them of a well-known importance in the pathophysiology of RA. This paper focuses on presenting the known mechanisms of resistance to malaria and their possible contribution to the pathophysiology of RA in this special group of patients.
2. The Role of Evolution and Natural Selection in the Development of the Immune System and Autoimmunity Phenomena
The human beings as well as all living species undergo evolutionary changes in response to natural selection in order to become more competitive favoring their survival. The immune system evolved primarily for defense against microorganisms and is comprised of various mechanisms that have been added over time. One of the older mechanisms is phagocytosis, characteristic of unicellular amebiform organisms. These ancient forms and primitive unicellular organisms acquired the ability to adhere and generate forms of intracellular signaling and specialization, thus generating cells with various functions configuring multicellular organisms or metazoans . Some cells continued to perform the function of phagocytic cells (sentinel) that we recognize today even in complex animals, such as mammals. Then through this tendency to cellular specialization, T cells and various molecules were generated to fulfill the work of defense such as cytokines or complement proteins. Through the time, mechanisms were added and a form of innate evolutionary memory was generated that together it has been called innate immune system. Later in the evolutionary process, it also acquired the ability to generate an immunological memory for the life of the individual, to recognize and eliminate pathogens in the future for those which are not innate forms of elimination. Thus either the acquired or adaptive immune system appears. The developing central nervous system which leads to the generation of other forms of memory is integrated in this process, which involves neurons and glial cells, implicated in tertiary forms of evolutionary memory, which in the context of immunity plays a very important role giving its connections to the immune and endocrine systems (neuro-endocrine-immune connections), that affects multiple forms of regulation and adaptation as well as various pathological conditions if there are changes in its performance. Individuals acquire social status and with it the development of a quaternary evolutionary memory or social memory, whose dysfunction causes various forms of diseases, including those related to the immune system . In this form of social memory, cultural aspects of humans are involved with multiple biological consequences, such as those associated with migration and displacement. This affects the evolutionary biology of individuals. In this paper we must take into account the genotypic and phenotypic differences that affect the presentation of RA in AD that developed in different geographical areas, such as North and South America [7, 8].
All aspects of cumulative evolution in the immune system mentioned above were developed in parallel with mechanisms that generated their regulation. Phagocytosis does its job and deregulation of its homeostatic mechanisms can lead to the development of several diseases (e.g., hemophagocytic syndrome). Also, disorders arising from deregulation of the complement system cause tissue injury due to immune complex deposition (e.g., lupus erythematosus, etc.). The simplest explanation for the existence of these regulatory mechanisms is the evolutionary accumulation that occurs parallel to immune defense mechanisms, in order to avoid self-harm .
Some of the known mechanisms by which autoimmune diseases develop is the alteration in the function of regulatory mechanisms. The RA does not escape this type of pathophysiological mechanisms, showing changes in molecular mechanisms such as cytokines, chemokines and adhesion molecules and cellular alterations of T and B lymphocytes.
3. Mechanisms of Resistance to Malaria
The mechanisms that confer resistance to malaria are the result of evolutionary changes conditioned by natural selection, being these changes, the strongest form of evolutionary pressure known in the recent history of humans . Most of these genetic changes confer resistance to malaria through mutations such as “loss of function” such as several hemoglobinopathies, which are the consequence of a punctual change of a nitrogenous base in one of the genes of hemoglobin. The major known changes that determine resistance or decrease in the severity of malaria caused by Plasmodium falciparum are the sickle cell trait (heterozygosity in the change of valine for glutamic acid at position 6 of the beta fraction of hemoglobin-Hb S) and beta-thalassemia (deficit in the synthesis of the beta chain of hemoglobin) . These changes create inhospitable conditions to the parasite that needs in red blood cell, the appropriate concentrations to survive, which are provided by normal hemoglobin. Other genetic alterations such as enzymopathies also confer resistance to malaria (deficiency of glucose-6-phosphate dehydrogenase or pyruvate kinase) .
Interestingly the number of modified evolutionarily molecules play important roles in the immune system. For example, a parasitic infection, as complex as Plasmodium, involves many immunological factors for its control. It depends on epidemiological factors, genetics, age, stage and parasite species, and duration of infection, among others. An individual can have multiple resistance factors and their combination determines different clinical presentations of infection. The immune response to acute infection, chronic exposure, or reinfection depends on changes that have occurred in the mechanisms of acquired immunity given by T and B lymphocytes. Specific antibody production can reduce for example, the severity of symptoms and mortality .
Several polymorphisms involved in immune response have been associated with resistance to malaria. Polymorphisms of class I HLA (HLA-Bw53) and class II HLA haplotype DRB1*1302-DQ B1*0501 are involved in resistance to malaria caused by Plasmodium falciparum . The polymorphism T232 of the Fc gamma receptor IIB (FcγRIIBT232) also confers resistance to malaria, particularly to severe forms of infection (cerebral malaria) caused by Plasmodium falciparum .
The complement receptor 1 (CR1, also called CD35) is a protein of 190–280 kDa located on the surface of red blood cells and belongs to the complement regulatory protein, responsible for removing immune complexes from the circulation . Some studies have suggested that PfEMP (P. falciparum erythrocyte membrane protein-1P), a membrane protein of Plasmodium falciparum, is a protein ligand of the CR1 and it could be involved in parasite rosette formation around erythrocytes, observed in vitro in forms of severe malaria and it could be also a pathogenic factor in these particular forms of disease . The CR1 gene encoding presents several polymorphisms that are involved in the amount of protein expression in the red cell membrane, and it would presumably confer protection, but reports in the literature are contradictory [18, 19], conferring protection apparently to severe forms of the disease such as the cerebral malaria.
The TNF-α is a cytokine with proinflammatory activity. It is produced mainly by monocytes and macrophages although T and B lymphocytes may also produce this cytokine. It plays an important role in inflammation and is relevant to autoimmune and infectious diseases . Several studies have suggested that TNF-α is an important mediator in the complications that accompany severe malaria by P. falciparum . Two gene promoter polymorphisms of TNF-α (homozygosity for the TNF-308A  and alleles of TNF-376A ) have been associated with cerebral malaria in children in Gambia and Kenya (Africa).
In the case of infections caused by Plasmodium vivax the most studied evolutionary change that determines resistance is the genetic polymorphism of parasite receptor known as Duffy Antigen Receptor for Chemokines (DARC) [24, 25], in which form of absent alleles does not allow the receipt and entry of the parasite to the red cell.
4. Mechanisms of Resistance to Malaria and Their Possible Role in the Presence and/or Severity of RA
Based on case reports and series of patients with sickle traits and beta-thalassemias, there are no changes in the presence or in the natural history of RA. Clinical presentation of RA may occur slightly more severe for their possible association with arthropathy associated with sickle cell disease . Little information is available about the role of asplenia (a condition related to these hemoglobinopathies) and RA. In the spleen, the immune complexes are cleared and the asplenia induced by hemoglobinopathies may influence the clinical course of diseases where these complexes play a major pathogenic role . To our knowledge there are not reports in the medical literature of patients with enzymopathies as deficiencies of glucose-6-phosphate dehydrogenase or pyruvate kinase, and the relation to the development or progression of autoimmune diseases, except as related to the worsening of anemic condition common in these pathologies .
In the same perspective, there is no information that associates either the HLA class I, HLA-Bw53 or HLA class II haplotype DRB1*1302-DQ B1*0501, with RA or other autoimmune or inflammatory phenomenon such as spondyloarthropathies .
There are three classes of FcγR: FcγRI (CD64), FcγRII (CD32) and FcγRIII (CD16). FcγRII class has several isoforms named as IIA, IIB, and IIC. All these receptors except FcγRIIB isoform have activating functions given the presence of “ITAM” (immunoreceptor tyrosine activation motif) able to phosphorylate through the help of protein-tyrosine kinases (PTK), and thus they lead to the activation of intracellular proteins that are designed to promote the action of transcription factors that induce the formation of proinflammatory cytokines and amplification of the immune response .
FcγRIIB isoform has inhibitory function by possessing “ITIMs,” which are inhibitory or regulatory forms of the immune response . The substitution of threonine for isoleucine at position 232 in the transmembrane domain known as FcγRIIBT232 determines an alteration in the function of this regulator receptor, which leads to an increase in immune reactivity mainly mediated by B lymphocytes and it is associated with the development of autoimmunity in experimental models and in humans. This polymorphism has also been correlated with the development of less severe malaria in animals and humans [15, 27]. Evolutionarily, a resistance to severe malaria has occurred in this case, but an increase in the development of autoimmune phenomena such as systemic lupus erythematosus (SLE) has been observed [31–35]. It is unknown whether this polymorphism is related to the development of RA, where the role of B lymphocytes is crucial for their development .
CR1 deficiency has been also associated with susceptibility to SLE , whose pathogenic factor would be the lack of clearance of immune complexes. A special relationship in RA patients has not been found yet. Some patients with RA show a decrease in expression of CR1 on the red blood cells, but it seems to be an acquired phenomenon .
Polymorphisms of TNF-α have been associated with the development of RA . TNF is a fundamental cytokine in the development of RA. Furthermore, TNF-308A single nucleotide polymorphism has been associated with radiological damage in RA patients. This association may be due to higher production of TNF associated with this polymorphism. Pharmacogenomics may be important because some of the TNF polymorphisms are associated with low response to anti-TNF therapies .
Concerning the susceptibility to Plasmodium vivax infection, there are two kinds of alleles related to the receptors DARC: Fya and Fyb, which identifies four possible phenotypic presentations: homozygous Fy (ab−) (absence of the receiver or null), homozygous Fy (a+ b+) and heterozygous Fy (a− b+) and Fy (a+ b−). These receptors belong to the family of seven transmembrane molecules, initially recognized as a receptor for the Plasmodium vivax in human red blood cells and the simian Plasmodium Knowlesi and then recognized as a “promiscuous” receptor which is able to bind both CC and CXC chemokines and to have a cleaner role of these molecules . Several chemokines related to the inflammatory process of RA are ligands of DARC, such as the CXC type chemokine, the interleukin-8 (IL-8) and neutrophil-activating protein derived from epithelial cells (ENA-78: epithelial cell-derived neutrophil-activating protein-78), and the CC type, such as chemoattractant protein of monocyte (MCP-1 monocyte chemoattractant protein-1) and the regulated protein of T lymphocytes expressed and secreted in normal activation (RANTES: regulated on activation normal T-cell expressed and secreted). The DARC expressed on endothelial cells of the synovium is important for the recruitment of neutrophils in patients with RA [42–50]. However, the role of DARC in the pathogenesis of RA is unknown. As it had been already mentioned, the DARC in this location has a role in clearance of circulating chemokines, a condition that could have an implication in the regulation of inflammatory processes. The phenotypes of the DARC have been studied in Caucasian patients from Italy with Behçet’s disease, where the chemokines IL-8 and MCP-1 may be important in the pathogenesis. In this study, there was no association among the genetic polymorphisms of these genes and the presence of the disease . It can be assumed that the absence or deficiency of the DARC would be related to more severe forms of RA.
Finally, some subsets of intermediate affinity T cells have been identified as associated with resistance to malaria and also to an autoimmune-like condition induced during infection . Although it is unknown whether these changes in cellular immunity are associated with RA, they can play, eventually, a role in individuals with this type of resistance to malaria.
Table 1 summarizes the mechanisms associated to malaria resistance, its role in regulating the immune system, and its possible role in autoimmune phenomena such as RA.
The evolutionary pressure in African ancestrally exposed to malaria has conditioned several changes at the molecular and cellular level generating difficulties for the reception of the parasite, metabolism, its possible removal by immune mechanisms and regulation of the inflammatory response to avoid damage to vital tissues like the brain. Some of these known and other putative changes can modify the development and progression of autoimmune diseases such as RA. Many pathophysiological factors are common among individuals with RA; however, these factors may be particular in individuals with ancestral exposure to malaria and mechanisms of resistance to it.
- D. L. Scott, D. P. M. Symmons, B. L. Coulton, and A. J. Popert, “Long-term outcome of treating rheumatoid arthritis: results after 20 years,” The Lancet, vol. 1, no. 8542, pp. 1108–1110, 1987.
- M. Lorenzo, “Rheumatoid arthritis,” Foot and Ankle Clinics, vol. 12, no. 3, pp. 525–537, 2007.
- D. L. Scott, F. Wolfe, and T. W. J. Huizinga, “Rheumatoid arthritis,” The Lancet, vol. 376, no. 9746, pp. 1094–1108, 2010.
- J. T. Birch Jr. and S. Bhattacharya, “Emerging trends in diagnosis and treatment of rheumatoid arthritis,” Primary Care, vol. 37, no. 4, pp. 779–792, 2010.
- N. King, C. T. Hittinger, and S. B. Carroll, “Evolution of key cell signaling and adhesion protein families predates animal origins,” Science, vol. 301, no. 5631, pp. 361–363, 2003.
- R. Dawkins, The Greatest Show on Earth, Free Press, New York, NY, USA, 2009.
- J. M. Anaya, P. A. Correa, R. D. Mantilla, F. Jimenez, T. Kuffner, and J. M. McNicholl, “Rheumatoid arthritis in African Colombians from Quibdo,” Seminars in Arthritis and Rheumatism, vol. 31, no. 3, pp. 191–198, 2001.
- G. S. Alarcoacuten, “Is rheumatoid arthritis in African descendants from North and South America the same?” Seminars in Arthritis and Rheumatism, vol. 31, no. 3, pp. 143–145, 2001.
- C. A. Cañas and F. Cañas, “The biological significance of evolution in autoimmune phenomena,” Autoimmune Diseases, vol. 2012, Article ID 784315, 12 pages, 2012.
- S. A. Tishkoff and S. M. Williams, “Genetic analysis of African populations: human evolution and complex disease,” Nature Reviews Genetics, vol. 3, no. 8, pp. 611–621, 2002.
- X. I. Pliakou, F. P. Koutsouka, D. Damigos, K. L. Bourantas, E. C. Briasoulis, and P. V. Voulgari, “Rheumatoid arthritis in patients with hemoglobinopathies,” Rheumatology International, vol. 32, no. 9, pp. 2889–2892, 2012.
- G. Min-Oo and P. Gros, “Erythrocyte variants and the nature of their malaria protective effect,” Cellular Microbiology, vol. 7, no. 6, pp. 753–763, 2005.
- T. G. Smith, K. Ayi, L. Serghides, C. D. Mcallister, and K. C. Kain, “Innate immunity to malaria caused by Plasmodium falciparum,” Clinical and Investigative Medicine, vol. 25, no. 6, pp. 262–272, 2002.
- C. López, C. Saravia, A. Gomez, J. Hoebeke, and M. A. Patarroyo, “Mechanisms of genetically-based resistance to malaria,” Gene, vol. 467, no. 1-2, pp. 1–12, 2010.
- A. Driss, J. M. Hibbert, N. O. Wilson, S. A. Iqbal, T. V. Adamkiewicz, and J. K. Stiles, “Genetic polymorphisms linked to susceptibility to malaria,” Malaria Journal, vol. 10, article 271, 2011.
- M. L. Reinagel, M. Gezen, P. J. Ferguson, S. Kuhn, E. N. Martin, and R. P. Taylor, “The primate erythrocyte complement receptor (CR1) as a privileged site: binding of immunoglobulin G to erythrocyte CR1 does not target erythrocytes for phagocytosis,” Blood, vol. 89, no. 3, pp. 1068–1077, 1997.
- T. N. Williams, “Red blood cell defects and malaria,” Molecular and Biochemical Parasitology, vol. 149, no. 2, pp. 121–127, 2006.
- V. Thathy, J. M. Moulds, B. Guyah, W. Otieno, and J. A. Stoute, “Complement receptor 1 polymorphisms associated with resistance to severe malaria in Kenya,” Malaria Journal, vol. 4, article 54, 2005.
- E. Nagayasu, M. Ito, M. Akaki et al., “CR1 density polymorphism on erythrocytes of falciparum malaria patients in Thailand,” American Journal of Tropical Medicine and Hygiene, vol. 64, no. 1-2, pp. 1–5, 2001.
- J. P. Bayley, T. H. M. Ottenhoff, and C. L. Verweij, “Is there a future for TNF promoter polymorphisms?” Genes and Immunity, vol. 5, no. 5, pp. 315–329, 2004.
- M. Odeh, “The role of tumour necrosis factor-α in the pathogenesis of complicated Falciparum malaria,” Cytokine, vol. 14, no. 1, pp. 11–18, 2001.
- J. C. Knight, I. Udalova, A. V. S. Hill et al., “A polymorphism that affects OCT-1 binding to the TNF promoter region is associated with severe malaria,” Nature Genetics, vol. 22, no. 2, pp. 145–150, 1999.
- D. Kwiatkowski, “Genetic susceptibility to malaria getting complex,” Current Opinion in Genetics and Development, vol. 10, no. 3, pp. 320–324, 2000.
- P. W. Hedrick, “Population genetics of malaria resistance in humans,” Heredity, vol. 107, pp. 283–304, 2011.
- D. P. Kwiatkowski, “How malaria has affected the human genome and what human genetics can teach us about malaria,” American Journal of Human Genetics, vol. 77, no. 2, pp. 171–192, 2005.
- K. Nistala and K. J. Murray, “Co-existent sickle cell disease and juvenile rheumatoid arthritis. Two cases with delayed diagnosis and severe destructive arthropathy,” Journal of Rheumatology, vol. 28, no. 9, pp. 2125–2128, 2001.
- M. R. Clatworthy, L. Willcocks, B. Urban et al., “Systemic lupus erythematosus-associated defects in the inhibitory receptor FcγRIIb reduce susceptibility to malaria,” Proceedings of the National Academy of Sciences of the United States of America, vol. 104, no. 17, pp. 7169–7174, 2007.
- V. Khurana and T. P. Bradley, “Adult-onset Still's disease associated with G6PD deficiency: a case report and literature review,” Journal of the Association for Academic Minority Physicians, vol. 9, no. 3, pp. 56–58, 1998.
- A. Chatzikyriakidou, P. V. Voulgari, and A. A. Drosos, “What is the role of HLA-B27 in spondyloarthropathies?” Autoimmunity Reviews, vol. 10, no. 8, pp. 464–468, 2011.
- L. M. Gómez, C. Cañas, and J. M. Anaya, “Fcy receptors and autoimmunity,” Acta Médica Colombiana, vol. 30, pp. 27–35, 2005.
- C. Kyogoku, H. M. Dijstelbloem, N. Tsuchiya et al., “Fcγ receptor gene polymorphisms in Japanese patients with systemic lupus erythematosus: contribution of FCGR2B to genetic susceptibility,” Arthritis and Rheumatism, vol. 46, no. 5, pp. 1242–1254, 2002.
- U. Siriboonrit, N. Tsuchiya, M. Sirikong et al., “Association of Fcγ receptor IIb and IIIb polymorphisms with susceptibility to systemic lupus erythematosus in Thais,” Tissue Antigens, vol. 61, no. 5, pp. 374–383, 2003.
- M. Waisberg, T. Tarasenko, B. K. Vickers et al., “Genetic susceptibility to systemic lupus erythematosus protects against cerebral malaria in mice,” Proceedings of the National Academy of Sciences of the United States of America, vol. 108, no. 3, pp. 1122–1127, 2011.
- L. C. Willcocks, E. J. Carr, H. A. Niederer et al., “A defunctioning polymorphism in FCGR2B is associated with protection against malaria but susceptibility to systemic lupus erythematosus,” Proceedings of the National Academy of Sciences of the United States of America, vol. 107, no. 17, pp. 7881–7885, 2010.
- K. G. C. Smith and M. R. Clatworthy, “FcγRIIB in autoimmunity and infection: evolutionary and therapeutic implications,” Nature Reviews Immunology, vol. 10, no. 5, pp. 328–343, 2010.
- T. Tiller, J. Kofer, C. Kreschel et al., “Development of self-reactive germinal center B cells and plasma cells in autoimmune FcγRIIB-deficient mice,” Journal of Experimental Medicine, vol. 207, no. 12, pp. 2767–2778, 2010.
- S. K. Nath, J. B. Harley, and Y. H. Lee, “Polymorphisms of complement receptor 1 and interleukin-10 genes and systemic lupus erythematosus: a meta-analysis,” Human Genetics, vol. 118, no. 2, pp. 225–234, 2005.
- A. Kumar, A. N. Malaviya, S. Sinha, P. S. Khandekar, K. Banerjee, and L. M. Srivastava, “C3b receptor (CR1) genomic polymorphism in rheumatoid arthritis: low receptor levels on erythrocytes are an acquired phenomenon,” Immunologic Research, vol. 13, no. 1, pp. 61–71, 1994.
- D. Khanna, H. Wu, G. Park et al., “Association of tumor necrosis factor α polymorphism, but not the shared epitope, with increased radiographic progression in a seropositive rheumatoid arthritis inception cohort,” Arthritis and Rheumatism, vol. 54, no. 4, pp. 1105–1116, 2006.
- Y. H. Lee, Y. H. Rho, S. J. Choi, J. D. Ji, and G. G. Song, “Association of TNF-alpha -308 G/A polymorphism with responsiveness to TNF-α-blockers in rheumatoid arthritis: a meta-analysis,” Rheumatology International, vol. 27, no. 2, pp. 157–161, 2006.
- G. J. Graham, M. Locati, A. Mantovani, A. Rot, and M. Thelen, “The biochemistry and biology of the atypical chemokine receptors,” Immunology Letters, vol. 145, no. 1-2, pp. 30–38, 2012.
- S. Hosaka, T. Akahoshi, C. Wada, and H. Kondo, “Expression of the chemokine superfamily in rheumatoid arthritis,” Clinical and Experimental Immunology, vol. 97, no. 3, pp. 451–457, 1994.
- T. Akahoshi, H. Endo, H. Kondo et al., “Essential involvement of interleukin-8 in neutrophil recruitment in rabbits with acute experimental arthritis induced by lipopolysaccharide and interleukin-1,” Lymphokine and Cytokine Research, vol. 13, no. 2, pp. 113–116, 1994.
- M. H. Yang, F. X. Wu, C. M. Xie et al., “Expression of CC chemokine ligand 5 in patients with rheumatoid arthritis and its correlation with disease activity and medication,” Chinese Medical Sciences Journal, vol. 24, no. 1, pp. 50–54, 2009.
- M. Norii, M. Yamamura, M. Iwahashi, A. Ueno, J. Yamana, and H. Makino, “Selective recruitment of CXCR3+ and CCR5+ CD4+ T cells into synovial tissue in patients with rheumatoid arthritis,” Acta Medica Okayama, vol. 60, no. 3, pp. 149–157, 2006.
- V. Pokorny, F. McQueen, S. Yeoman et al., “Evidence for negative association of the chemokine receptor CCR5 d32 polymorphism with rheumatoid arthritis,” Annals of the Rheumatic Diseases, vol. 64, no. 3, pp. 487–490, 2005.
- S. K. Lin, H. H. Chang, Y. J. Chen et al., “Epigallocatechin-3-gallate diminishes CCL2 expression in human osteoblastic cells via up-regulation of phosphatidylinositol 3-kinase/Akt/Raf-1 interaction: a potential therapeutic benefit for arthritis,” Arthritis and Rheumatism, vol. 58, no. 10, pp. 3145–3156, 2008.
- D. Smolarek, O. Bertrand, M. Czerwinski, Y. Colin, C. Etchebest, and A. G. de Brevern, “Multiple interests in structural models of DARC transmembrane protein,” Transfusion Clinique et Biologique, vol. 17, no. 3, pp. 184–196, 2010.
- A. M. Patterson, H. Siddall, G. Chamberlain, L. Gardner, and J. Middleton, “Expression of the Duffy antigen/receptor for chemokines (DARC) by the inflamed synovial endothelium,” Journal of Pathology, vol. 197, no. 1, pp. 108–116, 2002.
- E. Smith, H. M. McGettrick, M. A. Stone et al., “Duffy antigen receptor for chemokines and CXCL5 are essential for the recruitment of neutrophils in a multicellular model of rheumatoid arthritis synovium,” Arthritis and Rheumatism, vol. 58, no. 7, pp. 1968–1973, 2008.
- V. Pittoni, S. Vaglio, L. Magrini et al., “Polymorphism of the Duffy erythrocyte chemokine receptor in Italian patients with Behçet's disease,” Rheumatology International, vol. 23, no. 3, pp. 116–120, 2003.
- M. K. Mannoor, A. Weerasinghe, R. C. Halder et al., “Resistance to malarial infection is achieved by the cooperation of NK1.1+ and NK1.1- Subsets of intermediate TCR cells which are constituents of innate immunity,” Cellular Immunology, vol. 211, no. 2, pp. 96–104, 2001.