The T helper (Th) cell pool is composed of specialized cells with heterogeneous effector functions. Apart from Th1 and 2 cells, CXCR5+ T cells have been suggested to be another type of effector T cell specialized for B cell help. We show here that CXCR5+ T cells are heterogeneous, and we identify subsets of CXCR5+ CD4 T cells that differ in function and microenvironmental localization in secondary lymphoid tissues. CD57+CXCR5 T cells, hereafter termed germinal center Th (GC-Th) cells, are localized only in GCs, lack CCR7, and are highly responsive to the follicular chemokine B lymphocyte chemoattractant but not to the T cell zone EBI1-ligand chemokine. Importantly, GC-Th cells are much more efficient than CD57−CXCR5+ T cells or CXCR5− T cells in inducing antibody production from B cells. Consistent with their function, GC-Th cells produce elevated levels of interleukin 10 upon stimulation which, with other cytokines and costimulatory molecules, may help confer their B cell helper activity. Our results demonstrate that CXCR5+ T cells are functionally heterogeneous and that the GC-Th cells, a small subset of CXCR5+ T cells, are the key helpers for B cell differentiation and antibody production in lymphoid tissues.
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18 June 2001
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June 18 2001
Subspecialization of Cxcr5+ T Cells: B Helper Activity Is Focused in a Germinal Center–Localized Subset of Cxcr5+ T Cells
Chang H. Kim,
Chang H. Kim
aLaboratory of Immunology and Vascular Biology, Department of Pathology, Stanford University School of Medicine, Stanford, California 94305
bCenter for Molecular Biology and Medicine, Veterans Affairs Palo Alto Health Care System, Palo Alto, California 94304
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Lusijah S. Rott,
Lusijah S. Rott
aLaboratory of Immunology and Vascular Biology, Department of Pathology, Stanford University School of Medicine, Stanford, California 94305
bCenter for Molecular Biology and Medicine, Veterans Affairs Palo Alto Health Care System, Palo Alto, California 94304
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Ian Clark-Lewis,
Ian Clark-Lewis
cBiomedical Research Centre, University of British Columbia, Vancouver, British Columbia, Canada BC V6T 1Z3
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Daniel J. Campbell,
Daniel J. Campbell
aLaboratory of Immunology and Vascular Biology, Department of Pathology, Stanford University School of Medicine, Stanford, California 94305
bCenter for Molecular Biology and Medicine, Veterans Affairs Palo Alto Health Care System, Palo Alto, California 94304
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Lijun Wu,
Lijun Wu
dMillennium Pharmaceuticals, Incorporated, Cambridge, Massachusetts 02139
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Eugene C. Butcher
Eugene C. Butcher
aLaboratory of Immunology and Vascular Biology, Department of Pathology, Stanford University School of Medicine, Stanford, California 94305
bCenter for Molecular Biology and Medicine, Veterans Affairs Palo Alto Health Care System, Palo Alto, California 94304
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Chang H. Kim
aLaboratory of Immunology and Vascular Biology, Department of Pathology, Stanford University School of Medicine, Stanford, California 94305
bCenter for Molecular Biology and Medicine, Veterans Affairs Palo Alto Health Care System, Palo Alto, California 94304
Lusijah S. Rott
aLaboratory of Immunology and Vascular Biology, Department of Pathology, Stanford University School of Medicine, Stanford, California 94305
bCenter for Molecular Biology and Medicine, Veterans Affairs Palo Alto Health Care System, Palo Alto, California 94304
Ian Clark-Lewis
cBiomedical Research Centre, University of British Columbia, Vancouver, British Columbia, Canada BC V6T 1Z3
Daniel J. Campbell
aLaboratory of Immunology and Vascular Biology, Department of Pathology, Stanford University School of Medicine, Stanford, California 94305
bCenter for Molecular Biology and Medicine, Veterans Affairs Palo Alto Health Care System, Palo Alto, California 94304
Lijun Wu
dMillennium Pharmaceuticals, Incorporated, Cambridge, Massachusetts 02139
Eugene C. Butcher
aLaboratory of Immunology and Vascular Biology, Department of Pathology, Stanford University School of Medicine, Stanford, California 94305
bCenter for Molecular Biology and Medicine, Veterans Affairs Palo Alto Health Care System, Palo Alto, California 94304
Abbreviations used in this paper: BCA, B cell–attracting chemokine; BLC, B lymphocyte chemoattractant; ELC, EBI1-ligand chemokine; GC, germinal center; SDF, stromal cell–derived factor; SLC, secondary lymphoid tissue chemokine.
Received:
March 29 2001
Revision Requested:
May 04 2001
Accepted:
May 10 2001
Online ISSN: 1540-9538
Print ISSN: 0022-1007
© 2001 The Rockefeller University Press
2001
The Rockefeller University Press
J Exp Med (2001) 193 (12): 1373–1382.
Article history
Received:
March 29 2001
Revision Requested:
May 04 2001
Accepted:
May 10 2001
Citation
Chang H. Kim, Lusijah S. Rott, Ian Clark-Lewis, Daniel J. Campbell, Lijun Wu, Eugene C. Butcher; Subspecialization of Cxcr5+ T Cells: B Helper Activity Is Focused in a Germinal Center–Localized Subset of Cxcr5+ T Cells. J Exp Med 18 June 2001; 193 (12): 1373–1382. doi: https://doi.org/10.1084/jem.193.12.1373
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