Sustained T follicular helper cell response is essential for control of chronic viral infection
Author(s) -
Ute Greczmiel,
Nike Julia Kräutler,
Alessandro Pedrioli,
Ilka Bartsch,
Paola Agnellini,
Gregor Bedenikovic,
James A. Harker,
Kirsten Richter,
Annette Oxenius
Publication year - 2017
Publication title -
science immunology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 8.83
H-Index - 51
ISSN - 2470-9468
DOI - 10.1126/sciimmunol.aam8686
Subject(s) - immunology , follicular phase , chronic infection , cxcr5 , viral infection , biology , t helper cell , antibody , virology , antibody response , t cell , virus , b cell , immune system , germinal center , endocrinology
During chronic viral infections, both CD8 and CD4 T cell responses are functionally compromised. Alongside exhaustion of CD8 T cells during chronic viral infections, it has also been documented that the CD4 T cells have an increased propensity to differentiate toward CXCR5 + T follicular helper cell (T FH ) lineage. Whether these T FH cells contribute to the immune response to chronic viral infection has remained unclear. Using chronic lymphocytic choriomeningitis virus (LCMV) infection in conjunction with an in vivo system where T FH cells can be conditionally ablated, we have established that these T FH cells do in fact play an important protective function. Specifically, we demonstrate that these T FH cells are essential for the late emergence of neutralizing LCMV-specific antibodies that keep viral titers in check and ultimately allow mice to clear the virus. By supporting the generation of neutralizing antibodies, we show that sustained activity of T FH cells promotes control of the chronic infection in face of exhausted CD8 T cell responses.
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