Impaired antibody response to COVID-19 vaccination in advanced HIV infection

被引:57
|
作者
Hassold, Nolan [1 ]
Brichler, Segolene [2 ]
Ouedraogo, Elise [1 ]
Leclerc, Delphine [1 ]
Carroue, Sophie [1 ]
Gater, Yamina [2 ]
Alloui, Chakib [2 ]
Carbonnelle, Etienne [2 ,3 ,4 ]
Bouchaud, Olivier [1 ]
Mechai, Frederic [1 ,3 ,4 ]
Cordel, Hugues [1 ]
Delagreverie, Heloise [2 ,3 ,4 ]
机构
[1] Hop Avicenne, AP HP, Dept Infect & Trop Dis, Bobigny, France
[2] Hop Avicenne, AP HP, Dept Clin Microbiol, Bobigny, France
[3] Univ Sorbonne Paris Nord, INSERM, U1137, IAME, Paris, France
[4] Univ Paris, Paris, France
关键词
antibody; CD4(+) T cell; coronavirus disease 2019 vaccine; HIV-1; Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-COV-2); SARS-COV-2; IMMUNOGENICITY; SAFETY;
D O I
10.1097/QAD.0000000000003166
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objectives: Coronavirus disease 2019 (COVID-19) vaccination is reportedly efficient in people with HIV (PWH) but vaccine trials included participants with normal CD4(+) T-cell counts. We analyzed seroconversion rates and antibody titers following two-dose vaccination in PWH with impaired CD4(+) T-cell counts. Methods: We collected retrospective postvaccination SARS-COV-2 serology results available in a university hospital for PWH vaccinated between March and September, 2021 who were tested for antispike antibodies from 8 to 150 days following dose 2. Antibody titers were compared in PWH with CD4(+) T-cell count less than 200 cells/mu l, 200 Results: One hundred and five PWH were included: n = 54 in the CD4(+) T-cell count less than 500 cells/mu l group (n = 18 with CD4(+) <200 cells/mu l, n = 36 with 200 < CD4(+) < 500 cells/mu l) and 51 in the CD4(+) T-cell count greater than 500 cells/mu l group. They received two doses of BNT162b2 (75%), mRNA-1273 (8.5%), or ChAdOx1 nCoV-19 (16.5%). The median time from vaccine dose 2 to serology was consistent across all groups (73 days, interquartile range [29-97], P = 0.14). Seroconversion rates were 100% in the CD4(+) T-cell count greater than 500 cells/mu l group but 89% in participants with CD4(+) T-cell counts less than 500 cells/mu l (22 and 5.5% seronegative in the CD4(+) T-cell counts <200 cells/mu l and 200 < CD4(+) < 500 cells/mu l groups, respectively). Median antibody titers were 623.8 BAU/ml [262.2-2288] in the CD4(+) greater than 500 cells/mu l group versus 334.3 BAU/ml [69.9-933.9] in the CD4(+) less than 500 cells/mu l group (P = 0.003). They were lowest in the CD4(+) less than 200 cells/mu l group: 247.9 BAU/ml [5.88-434.9] (P = 0.0017) with only 44% achieving antibody titers above the putative protection threshold of 260 BAU/ml. Conclusion: PWH with CD4(+) T-cell counts less than 500 cells/mu l and notably less than 200 cells/mu l had significantly lower seroconversion rates and antispike antibody titers compared with PWH with CD4(+) T-cell counts greater than 500 cells/mu l, warranting the consideration of targeted vaccine strategies in this fragile population.
引用
收藏
页码:F1 / F5
页数:5
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