Broadly neutralizing plasma antibodies effective against autologous circulating viruses in infants with multivariant HIV-1 infection

被引:21
作者
Mishra, Nitesh [1 ]
Sharma, Shaifali [1 ]
Dobhal, Ayushman [1 ]
Kumar, Sanjeev [1 ,4 ]
Chawla, Himanshi [1 ,5 ,6 ]
Singh, Ravinder [2 ]
Makhdoomi, Muzamil Ashraf [1 ,7 ]
Das, Bimal Kumar [2 ]
Lodha, Rakesh [3 ]
Kabra, Sushil Kumar [3 ]
Luthra, Kalpana [1 ]
机构
[1] All India Inst Med Sci, Dept Biochem, New Delhi 110029, India
[2] All India Inst Med Sci, Dept Microbiol, New Delhi 110029, India
[3] All India Inst Med Sci, Dept Pediat, New Delhi 110029, India
[4] Int Ctr Genet Engn & Biotechnol, ICGEB Emory Vaccine Ctr, New Delhi, India
[5] Univ Southampton, Biol Sci, Southampton SO17 IBJ, Hants, England
[6] Univ Southampton, Inst Life, Southampton SO17 IBJ, Hants, England
[7] Cluster Univ, Govt Coll Women, Dept, Srinagar, India
关键词
EPITOPE; IDENTIFICATION; EVOLUTION; THERAPY; LINEAGE; VIREMIA;
D O I
10.1038/s41467-020-18225-x
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
Broadly neutralizing antibodies (bnAbs) develop in a subset of HIV-1 infected individuals over 2-3 years of infection. Infected infants develop plasma bnAbs frequently and as early as 1-year post-infection suggesting factors governing bnAb induction in infants are distinct from adults. Understanding viral characteristics in infected infants with early bnAb responses will provide key information about antigenic triggers driving B cell maturation pathways towards induction of bnAbs. Herein, we evaluate the presence of plasma bnAbs in a cohort of 51 HIV-1 Glade-C infected infants and identify viral factors associated with early bnAb responses. Plasma bnAbs targeting V2-apex on the env are predominant in infant elite and broad neutralizers. Circulating viral variants in infant elite neutralizers are susceptible to V2-apex bnAbs. In infant elite neutralizers, multivariant infection is associated with plasma bnAbs targeting diverse autologous viruses. Our data provides information supportive of polyvalent vaccination approaches capable of inducing V2-apex bnAbs against HIV-1.
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页数:11
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