Responses to Quadrivalent Influenza Vaccine Reveal Distinct Circulating CD4+CXCR5+T Cell Subsets in Men Living with HIV

被引:9
作者
Cole, Megan E. [1 ]
Saeed, Zainab [1 ]
Shaw, A. Torm [1 ]
Guo, Yanping [2 ]
Hoschler, Katja [3 ]
Winston, Alan [1 ,4 ]
Cooke, Graham S. [1 ]
Fidler, Sarah [1 ,4 ,6 ]
Taylor, Graham P. [1 ,5 ]
Pollock, Katrina M. [1 ,6 ]
机构
[1] Imperial Coll London, Virol Sect, Dept Infect Dis, London, England
[2] Imperial Coll London, St Marys FACS Facil, London, England
[3] Publ Hlth England, Resp Virus Unit, Virus Reference Dept, Natl Infect Serv, London, England
[4] Imperial Coll Healthcare NHS Trust, Clin Trials Ctr, Jefferiss Wing, London, England
[5] Imperial Coll Healthcare NHS Trust, Natl Ctr Human Retrovirol, London, England
[6] NIHR Imperial Biomed Res Ctr, London, England
关键词
INFECTION; CD32A; REPLICATION; FREQUENCY; EFFICACY; IMPACT;
D O I
10.1038/s41598-019-51961-9
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
T cell help for B cells may be perturbed in people living with HIV (PLWH), even when HIV is suppressed, as evidenced by reports of suboptimal responses to influenza vaccination. We investigated cT(FH) responses to the 2017-18 inactivated quadrivalent influenza vaccine (QIV) in men living with antiretroviral therapy (ART)-suppressed HIV infection who were treated in the early or chronic phase of infection, and control subjects. Here we show that seroprotective antibody responses in serum and oral fluid correlated with cTFH activation and were equivalent in all three groups, irrespective of when ART was started. These responses were attenuated in those reporting immunisation with influenza vaccine in the preceding three years, independent of HIV infection. Measurement of influenza-specific IgG in oral fluid was closely correlated with haemagglutination inhibition titre. T-SNE and two-dimensional analysis revealed a subset of CD4(+)CXCR3(+)CXCR5(+) cT(FH) activated at one week after vaccination. This was distinguishable from cTFH not activated by vaccination, and a rare, effector memory CD4(+)CXCR5(hi)CD32(hi) T cell subset. The data support the use of QIV for immunisation of PLWH, reveal distinct circulating CD4(+)CXCR5(+) T cell subsets and demonstrate oral fluid sampling for influenzaspecific IgG is an alternative to phlebotomy.
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