Perinatally Human Immunodeficiency Virus-Infected Adolescents and Young Adults Demonstrate Distinct BNT162b2 Messenger RNA Coronavirus Disease 2019 Vaccine Immunogenicity.
Perinatally Human Immunodeficiency Virus-Infected Adolescents and Young Adults Demonstrate Distinct BNT162b2 Messenger RNA Coronavirus Disease 2019 Vaccine Immunogenicity.
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DOI:
10.1093/cid/ciac408
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发表时间:
2022-08-15
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影响因子:
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Immunization of vulnerable populations with distinct immunity often results in suboptimal immunogenicity, durability, and efficacy. Safety and immunogenicity profiles of BNT162b2 messenger RNA coronavirus disease 2019 (COVID-19) vaccine, among people living with human immunodeficiency virus (HIV), were evaluated in 28 perinatally HIV-infected patients under antiretroviral therapy (ART) and 65 healthy controls (HCs) with no previous history of COVID-19. Thus, we measured severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)–specific humoral and CD4+ T cell responses. Samples were collected before vaccination (baseline, day [D] 0), at the second dose (D21), and at 4 weeks (D28) and 6 months (D180) after D0. Proteomic profiles at D0 and D28 were assessed with a multiplexed proximity extension assay (Olink) on plasma samples. All HIV-infected patients mounted similar anti–SARS-CoV-2 humoral responses to those of HCs, albeit with lower titers of anti-trimeric S at D28 (P = .01). Only peripheral blood mononuclear cells of HIV-infected patients demonstrated at D28 an impaired ability to expand their specific (CD40L+) CD4+ T-cell populations. Similar humoral titers were maintained between the 2 groups at 6-months follow-up. We additionally correlated baseline protein levels to either humoral or cellular responses, identifying clusters of molecules involved in immune response regulation with inverse profiles between the 2 study groups. Responses of ART-treated HIV-infected patients, compared to those of HCs, were characterized by distinct features especially within the proteomic compartment, supporting their eligibility to an additional dose, similarly to the HC schedule. In comparison to healthy individuals, perinatally HIV-infected patients with normal CD4 T-cell counts at the time of enrollment and with distinct baseline proteomic profiles mount and maintain specific immune responses upon BNT162b2 vaccination.
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DOI:
10.1056/nejmoa2034577
发表时间:
2020-12-31
期刊:
The New England journal of medicine
影响因子:
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作者:
Polack FP;Thomas SJ;Kitchin N;Absalon J;Gurtman A;Lockhart S;Perez JL;Pérez Marc G;Moreira ED;Zerbini C;Bailey R;Swanson KA;Roychoudhury S;Koury K;Li P;Kalina WV;Cooper D;Frenck RW Jr;Hammitt LL;Türeci Ö;Nell H;Schaefer A;Ünal S;Tresnan DB;Mather S;Dormitzer PR;Şahin U;Jansen KU;Gruber WC;C4591001 Clinical Trial Group
通讯作者:
C4591001 Clinical Trial Group
DOI:
10.1093/cid/ciaa1605
发表时间:
2021-10-05
期刊:
Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
影响因子:
--
作者:
Geretti AM;Stockdale AJ;Kelly SH;Cevik M;Collins S;Waters L;Villa G;Docherty A;Harrison EM;Turtle L;Openshaw PJM;Baillie JK;Sabin CA;Semple MG
通讯作者:
Semple MG
影响因子:
7.3
作者:
Amodio D;Ruggiero A;Sgrulletti M;Pighi C;Cotugno N;Medri C;Morrocchi E;Colagrossi L;Russo C;Zaffina S;Di Matteo G;Cifaldi C;Di Cesare S;Rivalta B;Pacillo L;Santilli V;Giancotta C;Manno EC;Ciofi Degli Atti M;Raponi M;Rossi P;Finocchi A;Cancrini C;Perno CF;Moschese V;Palma P
通讯作者:
Palma P
影响因子:
12.7
作者:
Xing, Mingluan;Feng, Yonghui;Lou, Xiaoming
通讯作者:
Lou, Xiaoming
影响因子:
7.3
作者:
Zhao J;Schank M;Wang L;Li Z;Nguyen LN;Dang X;Cao D;Khanal S;Nguyen LNT;Thakuri BKC;Ogbu SC;Lu Z;Wu XY;Morrison ZD;Gazzar ME;Liu Y;Zhang J;Ning S;Moorman JP;Yao ZQ
通讯作者:
Yao ZQ