Pre-existing infant antibody-dependent cellular cytotoxicity associates with reduced HIV-1 acquisition and lower morbidity.
Pre-existing infant antibody-dependent cellular cytotoxicity associates with reduced HIV-1 acquisition and lower morbidity.
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预先存在的婴儿抗体依赖的细胞毒性与HIV-1感染减少和发病率降低有关。
DOI:
10.1016/j.xcrm.2021.100412
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发表时间:
2021-10-19
期刊:
影响因子:
--
通讯作者:
Sagar M
中科院分区:
文献类型:
--
作者:
Thomas AS;Moreau Y;Jiang W;Isaac JE;Ewing A;White LF;Kourtis AP;Sagar M
In humans, pre-existing anti-HIV-1 neutralizing antibodies (nAbs) have not been associated with decreased HIV-1 acquisition. Here, we evaluate antibody-dependent cellular cytotoxicity (ADCC) present in pre-transmission infant and maternal plasma and breast milk (BM) against the contemporaneous maternal HIV-1 variants. HIV-1-exposed uninfected compared with HIV-1-exposed infected infants have higher ADCC and a combination of ADCC and nAb responses against their corresponding mother’s strains. ADCC does not correlate with nAbs, suggesting they are independent activities. The infected infants with high ADCC compared with low ADCC, but not those with higher ADCC plus nAbs, have lower morbidity up to 1 year after birth. A higher IgA to IgG ratio, observed in BM supernatants and in a higher proportion of the infected compared with the uninfected infants, associates with lower ADCC. Against the exposure strains, ADCC, more than nAbs, associates with both lower mother-to-child transmission and decreased post-infection infant morbidity. Infants with higher ADCC against their mother’s strains acquire HIV less frequently Infected infants with higher pre-transmission ADCC responses have better outcomes ADCC activity does not correlate with neutralizing antibody responses High IgA levels associate with lower ADCC activity Thomas et al. show that higher pre-existing ADCC responses against exposure strains associate with less likelihood of HIV-1 mother-to-child transmission and lower morbidity in infected infants.
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影响因子:
6.7
作者:
Kumar A;Smith CEP;Giorgi EE;Eudailey J;Martinez DR;Yusim K;Douglas AO;Stamper L;McGuire E;LaBranche CC;Montefiori DC;Fouda GG;Gao F;Permar SR
通讯作者:
Permar SR
DOI:
10.1126/science.aaf1279
发表时间:
2016-05-20
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Lu CL;Murakowski DK;Bournazos S;Schoofs T;Sarkar D;Halper-Stromberg A;Horwitz JA;Nogueira L;Golijanin J;Gazumyan A;Ravetch JV;Caskey M;Chakraborty AK;Nussenzweig MC
通讯作者:
Nussenzweig MC
DOI:
10.1056/nejmoa0911486
发表时间:
2010-06-17
期刊:
The New England journal of medicine
影响因子:
--
作者:
Chasela CS;Hudgens MG;Jamieson DJ;Kayira D;Hosseinipour MC;Kourtis AP;Martinson F;Tegha G;Knight RJ;Ahmed YI;Kamwendo DD;Hoffman IF;Ellington SR;Kacheche Z;Soko A;Wiener JB;Fiscus SA;Kazembe P;Mofolo IA;Chigwenembe M;Sichali DS;van der Horst CM;BAN Study Group
通讯作者:
BAN Study Group
影响因子:
2.7
作者:
Dudley, Dawn M.;Gao, Yong;Arts, Eric J.
通讯作者:
Arts, Eric J.
影响因子:
4.8
作者:
Hompe, Eliza D.;Jacobson, Denise L.;Permar, Sallie R.
通讯作者:
Permar, Sallie R.