D. Mcelroy, T. Ashley, D. Orazio, and S. , Lymphocytes serve as a reservoir for Listeria monocytogenes growth during infection of mice, Microbial Pathogenesis, vol.46, issue.4, pp.214-235, 2009.
DOI : 10.1016/j.micpath.2009.01.003

D. Thorley-lawson, Epstein-Barr virus: exploiting the immune system, Nature Reviews Immunology, vol.74, issue.1, pp.75-82, 2001.
DOI : 10.1038/35095584

Y. Liu, J. Zhang, P. Lane, E. Chan, and I. Maclennan, Sites of specific B cell activation in primary and secondary responses to T cell-dependent and T cell-independent antigens, European Journal of Immunology, vol.20, issue.12, pp.2951-62, 1991.
DOI : 10.1002/eji.1830211209

S. Nutt and D. Tarlinton, Germinal center B and follicular helper T cells: siblings, cousins or just good friends?, Nature Immunology, vol.179, issue.6, pp.472-479, 2011.
DOI : 10.1016/j.immuni.2009.12.005

L. Mcheyzer-williams, N. Pelletier, L. Mark, N. Fazilleau, and M. Mcheyzer-williams, Follicular helper T cells as cognate regulators of B cell immunity, Current Opinion in Immunology, vol.21, issue.3, pp.266-73, 2009.
DOI : 10.1016/j.coi.2009.05.010

S. Crotty, ), Annual Review of Immunology, vol.29, issue.1, pp.621-63, 2011.
DOI : 10.1146/annurev-immunol-031210-101400

S. Weller, M. Braun, B. Tan, A. Rosenwald, C. Cordier et al., Human blood IgM "memory" B cells are circulating splenic marginal zone B cells harboring a prediversified immunoglobulin repertoire, Blood, vol.104, issue.12, pp.3647-54, 2004.
DOI : 10.1182/blood-2004-01-0346

URL : https://hal.archives-ouvertes.fr/inserm-00338311

C. Garciadevinuesa, O. Leary, P. Sze, D. Toellner, K. Maclennan et al., T-independent type 2 antigens induce B cell proliferation in multiple splenic sites, but exponential growth is confined to extrafollicular foci, European Journal of Immunology, vol.90, issue.4, pp.1314-1337, 1999.
DOI : 10.1002/(SICI)1521-4141(199904)29:04<1314::AID-IMMU1314>3.0.CO;2-4

L. Wetzler, The role of Toll-like receptor 2 in microbial disease and immunity, Vaccine, vol.21, issue.2, pp.55-60, 2003.
DOI : 10.1016/S0264-410X(03)00201-9

I. Bekeredjian-ding, S. Inamura, T. Giese, H. Moll, S. Endres et al., Staphylococcus aureus Protein A Triggers T Cell-Independent B Cell Proliferation by Sensitizing B Cells for TLR2 Ligands, The Journal of Immunology, vol.178, issue.5, pp.2803-2815, 2007.
DOI : 10.4049/jimmunol.178.5.2803

A. Artz, W. Ershler, and D. Longo, Pneumococcal Vaccination and Revaccination of Older Adults, Clinical Microbiology Reviews, vol.16, issue.2, pp.308-326, 2003.
DOI : 10.1128/CMR.16.2.308-318.2003

G. Giebink, The Prevention of Pneumococcal Disease in Children, New England Journal of Medicine, vol.345, issue.16, pp.1177-83, 2001.
DOI : 10.1056/NEJMra010462

G. Overturf, Pneumococcal vaccination of children, Seminars in Pediatric Infectious Diseases, vol.13, issue.3, pp.155-64, 2002.
DOI : 10.1053/spid.2002.125858

W. Timens, A. Boes, T. Rozeboom-uiterwijk, and S. Poppema, Immaturity of the human splenic marginal zone in infancy. Possible contribution to the deficient infant immune response, J Immunol, vol.143, issue.10, pp.3200-3206, 1989.

Y. Shi, T. Yamazaki, Y. Okubo, Y. Uehara, K. Sugane et al., Regulation of Aged Humoral Immune Defense against Pneumococcal Bacteria by IgM Memory B Cell, The Journal of Immunology, vol.175, issue.5, pp.3262-3269, 2005.
DOI : 10.4049/jimmunol.175.5.3262

Y. You, R. Myers, L. Freeberg, J. Foote, J. Kearney et al., Marginal Zone B Cells Regulate Antigen Capture by Marginal Zone Macrophages, The Journal of Immunology, vol.186, issue.4, pp.2172-81, 2011.
DOI : 10.4049/jimmunol.1002106

URL : http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3099422

Y. You, H. Zhao, Y. Wang, and R. Carter, Cutting Edge: Primary and Secondary Effects of CD19 Deficiency on Cells of the Marginal Zone, The Journal of Immunology, vol.182, issue.12, pp.7343-7350, 2009.
DOI : 10.4049/jimmunol.0804295

G. Cinamon, M. Zachariah, O. Lam, F. Jr, F. Cyster et al., Follicular shuttling of marginal zone B cells facilitates antigen transport, Nature Immunology, vol.106, issue.1, pp.54-62, 2008.
DOI : 10.1126/science.1136736

M. Perez-andres, C. Grosserichter-wagener, C. Teodosio, J. Van-dongen, A. Orfao et al., B cells: Figure 1., The Journal of Experimental Medicine, vol.153, issue.13, pp.2565-2571, 2011.
DOI : 10.1111/j.1365-3083.1988.tb01476.x

B. Verbinnen, K. Covens, L. Moens, I. Meyts, and X. Bossuyt, Human CD20+CD43+CD27+CD5??? B cells generate antibodies to capsular polysaccharides of Streptococcus pneumoniae, Journal of Allergy and Clinical Immunology, vol.130, issue.1, pp.272-277, 2012.
DOI : 10.1016/j.jaci.2012.04.040

A. Scholzen and R. Sauerwein, How malaria modulates memory: activation and dysregulation of B cells in Plasmodium infection, Trends in Parasitology, vol.29, issue.5, pp.252-62, 2013.
DOI : 10.1016/j.pt.2013.03.002

A. Asito, E. Piriou, W. Jura, C. Ouma, P. Odada et al., Suppression of circulating IgD+CD27+ memory B cells in infants living in a malaria-endemic region of Kenya, Malaria Journal, vol.10, issue.1, p.362, 2011.
DOI : 10.1186/1475-2875-10-362

A. Cunnington and E. Riley, Suppression of vaccine responses by malaria: insignificant or overlooked?, Expert Review of Vaccines, vol.9, issue.4, pp.409-438, 2010.
DOI : 10.1586/erv.10.16

P. Requena, J. Campo, A. Umbers, M. Ome, R. Wangnapi et al., Pregnancy and Malaria Exposure Are Associated with Changes in the B Cell Pool and in Plasma Eotaxin Levels, The Journal of Immunology, vol.193, issue.6, pp.2971-83, 2014.
DOI : 10.4049/jimmunol.1401037

E. Nduati, A. Gwela, H. Karanja, C. Mugyenyi, J. Langhorne et al., The Plasma Concentration of the B Cell Activating Factor Is Increased in Children With Acute Malaria, Journal of Infectious Diseases, vol.204, issue.6, pp.962-70, 2011.
DOI : 10.1093/infdis/jir438

A. Scholzen, A. Teirlinck, E. Bijker, M. Roestenberg, C. Hermsen et al., BAFF and BAFF Receptor Levels Correlate with B Cell Subset Activation and Redistribution in Controlled Human Malaria Infection, The Journal of Immunology, vol.192, issue.8, pp.3719-3748, 2014.
DOI : 10.4049/jimmunol.1302960

Y. Jeong, S. Hong, S. Cho, W. Lee, and S. Lee, Induction of IL-10-Producing CD1dhighCD5+ Regulatory B Cells following Babesia microti-Infection, PLoS ONE, vol.7, issue.10, p.46553, 2012.
DOI : 10.1371/journal.pone.0046553.g008

M. Yang, L. Sun, S. Wang, K. Ko, H. Xu et al., Cutting Edge: Novel Function of B Cell-Activating Factor in the Induction of IL-10-Producing Regulatory B Cells, The Journal of Immunology, vol.184, issue.7, pp.3321-3326, 2010.
DOI : 10.4049/jimmunol.0902551

R. Kumsiri, P. Potup, K. Chotivanich, S. Petmitr, T. Kalambaheti et al., Blood stage Plasmodium falciparum antigens induce T cell independent immunoglobulin production via B cell activation factor of the TNF family (BAFF) pathway, Acta Tropica, vol.116, issue.3, pp.217-243, 2010.
DOI : 10.1016/j.actatropica.2010.08.012

G. Weiss, P. Crompton, S. Li, L. Walsh, S. Moir et al., Atypical Memory B Cells Are Greatly Expanded in Individuals Living in a Malaria-Endemic Area, The Journal of Immunology, vol.183, issue.3, pp.2176-82, 2009.
DOI : 10.4049/jimmunol.0901297

M. Muellenbeck, B. Ueberheide, B. Amulic, A. Epp, D. Fenyo et al., neutralizing antibodies, The Journal of Experimental Medicine, vol.43, issue.2, pp.389-99, 2013.
DOI : 10.1371/journal.ppat.1000770

G. Weiss, E. Clark, S. Li, B. Traore, K. Kayentao et al., A Positive Correlation between Atypical Memory B Cells and Plasmodium falciparum Transmission Intensity in Cross-Sectional Studies in Peru and Mali, PLoS ONE, vol.183, issue.2009, p.15983, 2011.
DOI : 10.1371/journal.pone.0015983.g004

S. Portugal, D. Doumtabe, B. Traore, L. Miller, M. Troye-blomberg et al., B cell analysis of ethnic groups in Mali with differential susceptibility to malaria, Malaria Journal, vol.11, issue.1, p.162, 2012.
DOI : 10.1073/pnas.1001323107

G. Ehrhardt, R. Davis, J. Hsu, C. Leu, A. Ehrhardt et al., The inhibitory potential of Fc receptor homolog 4 on memory B cells, Proceedings of the National Academy of Sciences, vol.100, issue.23, pp.13489-94, 2003.
DOI : 10.1073/pnas.1935944100

G. Ehrhardt, J. Hsu, L. Gartland, C. Leu, S. Zhang et al., Expression of the immunoregulatory molecule FcRH4 defines a distinctive tissue-based population of memory B cells, The Journal of Experimental Medicine, vol.94, issue.6, pp.783-91, 2005.
DOI : 10.1016/j.bbrc.2003.11.177

S. Moir, J. Ho, A. Malaspina, W. Wang, A. Dipoto et al., Evidence for HIV-associated B cell exhaustion in a dysfunctional memory B cell compartment in HIV-infected viremic individuals, The Journal of Experimental Medicine, vol.70, issue.8, pp.1797-805, 2008.
DOI : 10.1128/JVI.79.17.11214-11224.2005

H. Sohn, P. Krueger, R. Davis, and S. Pierce, FcRL4 acts as an adaptive to innate molecular switch dampening BCR signaling and enhancing TLR signaling, Blood, vol.118, issue.24, pp.6332-6373, 2011.
DOI : 10.1182/blood-2011-05-353102

M. Shio, F. Kassa, M. Bellemare, and M. Olivier, Innate inflammatory response to the malarial pigment hemozoin. Microbes and infection, Institut Pasteur, vol.12, pp.12-13889, 2010.

N. Chaoul, C. Burelout, S. Peruchon, B. Van-buu, P. Laurent et al., Default in plasma and intestinal IgA responses during acute infection by simian immunodeficiency virus, Retrovirology, vol.9, issue.1, p.43, 2012.
DOI : 10.1186/1742-4690-8-24

URL : https://hal.archives-ouvertes.fr/inserm-00723225

J. Fontaine, J. Chagnon-choquet, H. Valcke, J. Poudrier, M. Roger et al., High expression levels of B lymphocyte stimulator (BLyS) by dendritic cells correlate with HIV-related B-cell disease progression in humans, Blood, vol.117, issue.1, pp.145-55, 2011.
DOI : 10.1182/blood-2010-08-301887

J. Allen and R. Maizels, Diversity and dialogue in immunity to helminths, Nature Reviews Immunology, vol.12, issue.6, pp.375-88, 2011.
DOI : 10.1038/nri2992

B. Everts, A. Adegnika, Y. Kruize, H. Smits, P. Kremsner et al., Functional Impairment of Human Myeloid Dendritic Cells during Schistosoma haematobium Infection, PLoS Neglected Tropical Diseases, vol.86, issue.4, p.667, 2010.
DOI : 10.1371/journal.pntd.0000667.t001

L. Labuda, U. Ateba-ngoa, E. Feugap, J. Heeringa, L. Van-der-vlugt et al., Alterations in Peripheral Blood B Cell Subsets and Dynamics of B Cell Responses during Human Schistosomiasis, PLoS Neglected Tropical Diseases, vol.209, issue.3, p.2094, 2013.
DOI : 10.1371/journal.pntd.0002094.s003

L. Van-der-vlugt, L. Labuda, A. Ozir-fazalalikhan, E. Lievers, A. Gloudemans et al., Schistosomes Induce Regulatory Features in Human and Mouse CD1dhi B Cells: Inhibition of Allergic Inflammation by IL-10 and Regulatory T Cells, PLoS ONE, vol.158, issue.2, p.30883, 2012.
DOI : 10.1371/journal.pone.0030883.s005

T. Positive, S. Cells, T. Effector, and . Cytokines, The Journal of infectious diseases, pp.1207-1223, 2014.

R. Dhiman, M. Indramohan, P. Barnes, R. Nayak, P. Paidipally et al., IL-22 Produced by Human NK Cells Inhibits Growth of Mycobacterium tuberculosis by Enhancing Phagolysosomal Fusion, The Journal of Immunology, vol.183, issue.10, pp.6639-6684, 2009.
DOI : 10.4049/jimmunol.0902587

S. Khader, G. Bell, J. Pearl, J. Fountain, J. Rangel-moreno et al., IL-23 and IL-17 in the establishment of protective pulmonary CD4+ T cell responses after vaccination and during Mycobacterium tuberculosis challenge, Nature Immunology, vol.175, issue.4, pp.369-77, 2007.
DOI : 10.1084/jem.20050193

Y. Okamoto-yoshida, M. Umemura, A. Yahagi, O. Brien, R. Ikuta et al., Essential Role of IL-17A in the Formation of a Mycobacterial Infection-Induced Granuloma in the Lung, The Journal of Immunology, vol.184, issue.8, pp.4414-4436, 2010.
DOI : 10.4049/jimmunol.0903332

M. Zhang, Z. Wang, M. Graner, L. Yang, M. Liao et al., B cell infiltration is associated with the increased IL-17 and IL-22 expression in the lungs of patients with tuberculosis, Cellular Immunology, vol.270, issue.2, pp.217-240, 2011.
DOI : 10.1016/j.cellimm.2011.05.009

M. Zhang, X. Zheng, J. Zhang, Y. Zhu, X. Zhu et al., CD19+CD1d+CD5+ B cell frequencies are increased in patients with tuberculosis and suppress Th17 responses, Cellular Immunology, vol.274, issue.1-2, pp.89-97, 2012.
DOI : 10.1016/j.cellimm.2012.01.007

Y. Souwer, A. Griekspoor, T. Jorritsma, J. De-wit, H. Janssen et al., B Cell Receptor-Mediated Internalization of Salmonella: A Novel Pathway for Autonomous B Cell Activation and Antibody Production, The Journal of Immunology, vol.182, issue.12, pp.7473-81, 2009.
DOI : 10.4049/jimmunol.0802831

M. Nanton, S. Way, M. Shlomchik, and S. Mcsorley, Cutting Edge: B Cells Are Essential for Protective Immunity against Salmonella Independent of Antibody Secretion, The Journal of Immunology, vol.189, issue.12, pp.5503-5510, 2012.
DOI : 10.4049/jimmunol.1201413

P. Shen, T. Roch, V. Lampropoulou, O. Connor, R. Stervbo et al., IL-35-producing B cells are critical regulators of immunity during autoimmune and infectious diseases, Nature, vol.42, issue.7492, pp.366-70, 2014.
DOI : 10.1038/nature12979

A. Malaspina, S. Moir, S. Kottilil, C. Hallahan, L. Ehler et al., Deleterious Effect of HIV-1 Plasma Viremia on B Cell Costimulatory Function, The Journal of Immunology, vol.170, issue.12, pp.5965-72, 2003.
DOI : 10.4049/jimmunol.170.12.5965

S. Moir and A. Fauci, B cells in HIV infection and disease, Nature Reviews Immunology, vol.90, issue.4, pp.235-280, 2009.
DOI : 10.1038/nri2524

K. Titanji, F. Chiodi, R. Bellocco, D. Schepis, L. Osorio et al., Primary HIV-1 infection sets the stage for important B lymphocyte dysfunctions, AIDS, vol.19, issue.17, pp.1947-55, 2005.
DOI : 10.1097/01.aids.0000191231.54170.89

A. Amadori and L. Chieco-bianchi, B-cell activation and HIV-1 infection: Deeds and misdeeds, Immunology Today, vol.11, issue.10, pp.374-383, 1990.
DOI : 10.1016/0167-5699(90)90144-X

H. Lane, H. Masur, L. Edgar, G. Whalen, A. Rook et al., Abnormalities of B-Cell Activation and Immunoregulation in Patients with the Acquired Immunodeficiency Syndrome, New England Journal of Medicine, vol.309, issue.8, pp.453-461, 1983.
DOI : 10.1056/NEJM198308253090803

F. Muller, S. Froland, and P. Brandtzaeg, Altered IgG-subclass distribution in lymph node cells and serum of adults infected with human immunodeficiency virus (HIV), Clin Exp Immunol, vol.78, issue.2, pp.153-161, 1989.

M. Bonsignori, S. Alam, H. Liao, L. Verkoczy, G. Tomaras et al., HIV-1 antibodies from infection and vaccination: insights for guiding vaccine design, Trends in Microbiology, vol.20, issue.11, pp.532-541, 2012.
DOI : 10.1016/j.tim.2012.08.011

J. Kobie, D. Alcena, B. Zheng, P. Bryk, J. Mattiacio et al., 9G4 Autoreactivity Is Increased in HIV-Infected Patients and Correlates with HIV Broadly Neutralizing Serum Activity, PLoS ONE, vol.48, issue.4, p.35356, 2012.
DOI : 10.1371/journal.pone.0035356.s005

M. Hart, A. Steel, S. Clark, G. Moyle, M. Nelson et al., Loss of Discrete Memory B Cell Subsets Is Associated with Impaired Immunization Responses in HIV-1 Infection and May Be a Risk Factor for Invasive Pneumococcal Disease, The Journal of Immunology, vol.178, issue.12, pp.8212-8232, 2007.
DOI : 10.4049/jimmunol.178.12.8212

K. Titanji, D. Milito, A. Cagigi, A. Thorstensson, R. Grutzmeier et al., Loss of memory B cells impairs maintenance of long-term serologic memory during HIV-1 infection, Blood, vol.108, issue.5, pp.1580-1587, 2006.
DOI : 10.1182/blood-2005-11-013383

S. Peruchon, N. Chaoul, C. Burelout, B. Delache, P. Brochard et al., Tissue-Specific B-Cell Dysfunction and Generalized Memory B-Cell Loss during Acute SIV Infection, PLoS ONE, vol.4, issue.6, p.5966, 2009.
DOI : 10.1371/journal.pone.0005966.s005

URL : http://doi.org/10.1371/journal.pone.0005966

B. He, X. Qiao, P. Klasse, A. Chiu, A. Chadburn et al., HIV-1 Envelope Triggers Polyclonal Ig Class Switch Recombination through a CD40-Independent Mechanism Involving BAFF and C-Type Lectin Receptors, The Journal of Immunology, vol.176, issue.7, pp.3931-3972, 2006.
DOI : 10.4049/jimmunol.176.7.3931

K. Good, D. Avery, and S. Tangye, Resting Human Memory B Cells Are Intrinsically Programmed for Enhanced Survival and Responsiveness to Diverse Stimuli Compared to Naive B Cells, The Journal of Immunology, vol.182, issue.2, pp.890-901, 2009.
DOI : 10.4049/jimmunol.182.2.890

K. Titanji, V. Velu, L. Chennareddi, M. Vijay-kumar, A. Gewirtz et al., Acute depletion of activated memory B cells involves the PD-1 pathway in rapidly progressing SIV-infected macaques, Journal of Clinical Investigation, vol.120, issue.11, pp.3878-90, 2010.
DOI : 10.1172/JCI43271DS1

L. Kardava, S. Moir, W. Wang, J. Ho, C. Buckner et al., Attenuation of HIV-associated human B cell exhaustion by siRNA downregulation of inhibitory receptors, Journal of Clinical Investigation, vol.121, issue.7, pp.2614-2638, 2011.
DOI : 10.1172/JCI45685DS1

K. Jelicic, R. Cimbro, F. Nawaz, W. Da-huang, X. Zheng et al., The HIV-1 envelope protein gp120 impairs B cell proliferation by inducing TGF-??1 production and FcRL4 expression, Nature Immunology, vol.132, issue.12, pp.1256-65, 2013.
DOI : 10.1038/ni.2746

C. Legendre, M. Raphael, G. Gras, E. Lefevre, J. Feuillard et al., CD80 expression is decreased in hyperplastic lymph nodes of HIV+ patients., International Immunology, vol.10, issue.12, pp.1847-51, 1998.
DOI : 10.1093/intimm/10.12.1847

G. Badr, G. Borhis, D. Treton, C. Moog, O. Garraud et al., HIV Type 1 Glycoprotein 120 Inhibits Human B Cell Chemotaxis to CXC Chemokine Ligand (CXCL) 12, CC Chemokine Ligand (CCL)20, and CCL21, The Journal of Immunology, vol.175, issue.1, pp.302-312, 2005.
DOI : 10.4049/jimmunol.175.1.302

K. Tenner-racz, H. Stellbrink, J. Van-lunzen, C. Schneider, J. Jacobs et al., The Unenlarged Lymph Nodes of HIV-1???infected, Asymptomatic Patients with High CD4 T Cell Counts Are Sites for Virus Replication and CD4 T Cell Proliferation. The Impact of Highly Active Antiretroviral Therapy, The Journal of Experimental Medicine, vol.151, issue.6, pp.949-59, 1998.
DOI : 10.1126/science.277.5322.112

G. Pantaleo, C. Graziosi, J. Demarest, O. Cohen, M. Vaccarezza et al., Role of Lymphoid Organs in the Pathogenesis of Human Immunodeficiency Virus (HIV) Infection, Immunological Reviews, vol.321, issue.1, pp.105-135, 1994.
DOI : 10.1016/S0140-6736(86)92808-4

M. Levesque, M. Moody, K. Hwang, D. Marshall, J. Whitesides et al., Polyclonal B Cell Differentiation and Loss of Gastrointestinal Tract Germinal Centers in the Earliest Stages of HIV-1 Infection, PLoS Medicine, vol.457, issue.10, p.1000107, 2009.
DOI : 10.1371/journal.pmed.1000107.s008

Z. Zhang, D. Casimiro, W. Schleif, M. Chen, M. Citron et al., Early depletion of proliferating B cells of germinal center in rapidly progressive simian immunodeficiency virus infection, Virology, vol.361, issue.2, pp.455-64, 2007.
DOI : 10.1016/j.virol.2006.12.006

J. Hong, P. Amancha, K. Rogers, A. Ansari, and F. Villinger, Spatial Alterations between CD4+ T Follicular Helper, B, and CD8+ T Cells during Simian Immunodeficiency Virus Infection: T/B Cell Homeostasis, Activation, and Potential Mechanism for Viral Escape, The Journal of Immunology, vol.188, issue.7, pp.3247-56, 2012.
DOI : 10.4049/jimmunol.1103138

M. Lindqvist, J. Van-lunzen, D. Soghoian, B. Kuhl, S. Ranasinghe et al., Expansion of HIV-specific T follicular helper cells in chronic HIV infection, Journal of Clinical Investigation, vol.122, issue.9, pp.3271-80, 2012.
DOI : 10.1172/JCI64314DS1

M. Perreau, A. Savoye, D. Crignis, E. Corpataux, J. Cubas et al., Follicular helper T cells serve as the major CD4 T cell compartment for HIV-1 infection, replication, and production, The Journal of Experimental Medicine, vol.9, issue.1, pp.143-56, 2013.
DOI : 10.1126/science.278.5341.1291

C. Petrovas, T. Yamamoto, M. Gerner, K. Boswell, K. Wloka et al., CD4 T follicular helper cell dynamics during SIV infection, Journal of Clinical Investigation, vol.122, issue.9, pp.3281-94, 2012.
DOI : 10.1172/JCI63039DS1

F. Yue, C. Lo, A. Sakhdari, E. Lee, C. Kovacs et al., HIV-Specific IL-21 Producing CD4+ T Cells Are Induced in Acute and Chronic Progressive HIV Infection and Are Associated with Relative Viral Control, The Journal of Immunology, vol.185, issue.1, pp.498-506, 2010.
DOI : 10.4049/jimmunol.0903915

W. Xu, P. Santini, J. Sullivan, B. He, M. Shan et al., HIV-1 evades virus-specific IgG2 and IgA responses by targeting systemic and intestinal B cells via long-range intercellular conduits, Nature Immunology, vol.393, issue.9, pp.1008-1025, 2009.
DOI : 10.1038/ni.1753

E. Lefevre, R. Krzysiek, E. Loret, P. Galanaud, and Y. Richard, Cutting edge: HIV-1 Tat protein differentially modulates the B cell response of naive, memory, and germinal center B cells, J Immunol, vol.163, issue.3, pp.1119-1141, 1999.

A. Malaspina, S. Moir, J. Ho, W. Wang, M. Howell et al., Appearance of immature/transitional B cells in HIV-infected individuals with advanced disease: Correlation with increased IL-7, Proceedings of the National Academy of Sciences, vol.103, issue.7, pp.2262-2269, 2006.
DOI : 10.1073/pnas.0511094103

W. Stohl, G. Cheema, W. Briggs, D. Xu, S. Sosnovtseva et al., B Lymphocyte Stimulator Protein-Associated Increase in Circulating Autoantibody Levels May Require CD4+ T Cells: Lessons from HIV-Infected Patients, Clinical Immunology, vol.104, issue.2, pp.115-137, 2002.
DOI : 10.1006/clim.2002.5238

Y. Richard, C. Amiel, V. Jeantils, D. Mestivier, A. Portier et al., Changes in Blood B Cell Phenotypes and Epstein???Barr Virus Load in Chronically Human Immunodeficiency Virus???Infected Patients before and after Antiretroviral Therapy, The Journal of Infectious Diseases, vol.202, issue.9, pp.1424-1458, 2010.
DOI : 10.1086/656479

URL : https://hal.archives-ouvertes.fr/hal-00560997

A. Gloghini, R. Dolcetti, and A. Carbone, Lymphomas occurring specifically in HIV-infected patients: From pathogenesis to pathology, Seminars in Cancer Biology, vol.23, issue.6, pp.457-67, 2013.
DOI : 10.1016/j.semcancer.2013.08.004

J. Pestka, M. Zeisel, E. Blaser, P. Schurmann, B. Bartosch et al., Rapid induction of virus-neutralizing antibodies and viral clearance in a single-source outbreak of hepatitis C, Proceedings of the National Academy of Sciences, vol.104, issue.14, pp.6025-6055, 2007.
DOI : 10.1073/pnas.0607026104

URL : https://hal.archives-ouvertes.fr/inserm-00395910

J. Herkel and A. Carambia, Let it B in viral hepatitis?, Journal of Hepatology, vol.55, issue.1, pp.5-7, 2011.
DOI : 10.1016/j.jhep.2010.12.027

M. Chen, M. Sallberg, A. Sonnerborg, O. Weiland, L. Mattsson et al., Limited humoral immunity in hepatitis C virus infection, Gastroenterology, vol.116, issue.1, pp.135-178, 1999.
DOI : 10.1016/S0016-5085(99)70237-4

H. Doi, S. Tanoue, and D. Kaplan, Peripheral CD27???CD21??? B-cells represent an exhausted lymphocyte population in hepatitis C cirrhosis, Clinical Immunology, vol.150, issue.2, pp.184-91, 2014.
DOI : 10.1016/j.clim.2013.12.001

B. Oliviero, A. Cerino, S. Varchetta, E. Paudice, S. Pai et al., Enhanced B-cell differentiation and reduced proliferative capacity in chronic hepatitis C and chronic hepatitis B virus infections, Journal of Hepatology, vol.55, issue.1, pp.53-60, 2011.
DOI : 10.1016/j.jhep.2010.10.016

D. Ducoulombier, A. Roque-afonso, D. Liberto, G. Penin, F. Kara et al., Frequent compartmentalization of hepatitis C virus variants in circulating B cells and monocytes, Hepatology, vol.187, issue.3, pp.817-842, 2004.
DOI : 10.1002/hep.20087

URL : https://hal.archives-ouvertes.fr/hal-00313691

M. Ito, H. Kusunoki, and T. Mizuochi, Peripheral B Cells as Reservoirs for Persistent HCV Infection, Frontiers in Microbiology, vol.2, p.177, 2011.
DOI : 10.3389/fmicb.2011.00177

E. Toubi, S. Gordon, A. Kessel, I. Rosner, M. Rozenbaum et al., Elevated serum B-Lymphocyte activating factor (BAFF) in chronic hepatitis C virus infection: Association with autoimmunity, Journal of Autoimmunity, vol.27, issue.2, pp.134-143, 2006.
DOI : 10.1016/j.jaut.2006.07.005

B. Lee, A. Tucker, L. Frelin, M. Sallberg, J. Jones et al., Interaction of the Hepatitis B Core Antigen and the Innate Immune System, The Journal of Immunology, vol.182, issue.11, pp.6670-81, 2009.
DOI : 10.4049/jimmunol.0803683