| Literature DB >> 26795249 |
Bruce T Schultz1, Jeffrey E Teigler2, Franco Pissani2, Alexander F Oster2, Gregory Kranias2, Galit Alter3, Mary Marovich2, Michael A Eller2, Ulf Dittmer4, Merlin L Robb2, Jerome H Kim5, Nelson L Michael6, Diane Bolton2, Hendrik Streeck7.
Abstract
A central effort in HIV vaccine development is to generate protective broadly neutralizing antibodies, a process dependent on T follicular helper (Tfh) cells. The feasibility of using peripheral blood counterparts of lymph node Tfh cells to assess the immune response and the influence of viral and vaccine antigens on their helper functions remain obscure. We assessed circulating HIV-specific IL-21(+)CD4(+) T cells and showed transcriptional and phenotypic similarities to lymphoid Tfh cells, and hence representing peripheral Tfh (pTfh) cells. pTfh cells were functionally active and B cell helper quality differed depending on antigen specificity. Furthermore, we found higher frequency of pTfh cells in peripheral blood mononuclear cell specimens from the ALVAC+AIDSVAX (RV144) HIV vaccine trial associated with protective antibody responses compared to the non-protective DNA+Ad5 vaccine trial. Together, we identify IL-21(+)CD4(+) T cells as pTfh cells, implicating them as key populations in the generation of vaccine-evoked antibody responses.Entities:
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Year: 2016 PMID: 26795249 DOI: 10.1016/j.immuni.2015.12.011
Source DB: PubMed Journal: Immunity ISSN: 1074-7613 Impact factor: 31.745