TY - JOUR
T1 - B cells in T follicular helper cell development and function
T2 - Separable roles in delivery of ICOS ligand and antigen
AU - Weinstein, Jason S.
AU - Bertino, Sarah A.
AU - Hernandez, Sairy G.
AU - Poholek, Amanda C.
AU - Teplitzky, Taylor B.
AU - Nowyhed, Heba N.
AU - Craft, Joe
PY - 2014/4/1
Y1 - 2014/4/1
N2 - B cells are required for follicular Th (Tfh) cell development, as is the ICOS ligand (ICOS-L); however, the separable contributions of Ag and ICOS-L delivery by cognate B cells to Tfh cell development and function are unknown.We find that Tfh cell and germinal center differentiation are dependent on cognate B cell display of ICOS-L, but only when Ag presentation by the latter is limiting, with the requirement for B cell expression of ICOS-L overcome by robust Ag delivery. These findings demonstrate that Ag-specific B cells provide different, yet compensatory, signals for Tfh cell differentiation, while reconciling conflicting data indicating a requirement for ICOS-L expression on cognate B cells for Tfh cell development with those demonstrating that the latter requirement could be bypassed in lieu of that tendered by noncognate B cells. Our findings clarify the separable roles of delivery of Ag and ICOS-L by cognate B cells for Tfh cell maturation and function, and have implications for using therapeutic ICOS blockade in settings of abundantly available Ag, such as in systemic autoimmunity. The Journal of Immunology, 2014, 192: 3166-3179.
AB - B cells are required for follicular Th (Tfh) cell development, as is the ICOS ligand (ICOS-L); however, the separable contributions of Ag and ICOS-L delivery by cognate B cells to Tfh cell development and function are unknown.We find that Tfh cell and germinal center differentiation are dependent on cognate B cell display of ICOS-L, but only when Ag presentation by the latter is limiting, with the requirement for B cell expression of ICOS-L overcome by robust Ag delivery. These findings demonstrate that Ag-specific B cells provide different, yet compensatory, signals for Tfh cell differentiation, while reconciling conflicting data indicating a requirement for ICOS-L expression on cognate B cells for Tfh cell development with those demonstrating that the latter requirement could be bypassed in lieu of that tendered by noncognate B cells. Our findings clarify the separable roles of delivery of Ag and ICOS-L by cognate B cells for Tfh cell maturation and function, and have implications for using therapeutic ICOS blockade in settings of abundantly available Ag, such as in systemic autoimmunity. The Journal of Immunology, 2014, 192: 3166-3179.
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U2 - 10.4049/jimmunol.1302617
DO - 10.4049/jimmunol.1302617
M3 - Article
C2 - 24610013
AN - SCOPUS:84897501021
SN - 0022-1767
VL - 192
SP - 3166
EP - 3179
JO - Journal of Immunology
JF - Journal of Immunology
IS - 7
ER -