Broad and potent cross clade neutralizing antibodies with multiple specificities in the plasma of HIV-1 subtype C infected individuals

被引:6
作者
Cheedarla, Narayanaiah [1 ]
Precilla, K. Lucia [1 ]
Babu, Hemalatha [1 ]
Vijayan, K. K. Vidya [1 ]
Ashokkumar, Manickam [1 ]
Chandrasekaran, Padmapriyadarsini [1 ]
Kailasam, Nandagopal [2 ]
Sundaramurthi, Jagadish Chandrabose [1 ]
Swaminathan, Soumya [1 ]
Buddolla, Viswanath [3 ]
Vaniambadi, S. Kalyanaraman [4 ]
Ramanathan, V. D. [1 ]
Hanna, Luke Elizabeth [1 ]
机构
[1] Natl Inst Res TB, HIV AIDS Div, Dept Clin Res, Clin Res, Madras 600031, Tamil Nadu, India
[2] Kilpauk Med Coll & Hosp, ART Ctr, Madras 600010, Tamil Nadu, India
[3] Gachon Univ, Dept Bionanotechnol, San 65, Seongnam Si 461701, Gyeonggi Do, South Korea
[4] Adv Biosci Labs Inc, Rockville, MD 20850 USA
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
关键词
B-CELLS; MONOCLONAL-ANTIBODIES; ENV CLONES; VACCINE; DESIGN; RESPONSES; EPITOPES; INSIGHTS; PG9;
D O I
10.1038/srep46557
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 Cross clade Neutralizing (BCN) antibodies are recognized as potential therapeutic tools and leads for the design of a vaccine that can protect human beings against various clades of Human Immunodeficiency Virus (HIV). In the present study, we screened plasma of 88 HIV-1 infected ART naive individuals for their neutralization potential using a standard panel of 18 pseudoviruses belonging to different subtypes and different levels of neutralization. We identified 12 samples with good breadth of neutralization (neutralized >90% of the viruses). Four of these samples neutralized even the difficult-to-neutralize tier-3 pseudoviruses with great potency (GMT > 600). Analysis of neutralization specificities indicated that four samples had antibodies with multiple epitope binding specificities, viz. CD4-binding site (CD4BS), glycans in the V1/V2 and V3 regions and membrane proximal external region (MPER). Our findings indicate the strong possibility of identifying highly potent bNAbs with known or novel specificities from HIV-1 subtype C infected individuals from India that can be exploited as therapeutic tools or lead molecules for the identification of potential epitopes for design of a protective HIV-1 vaccine.
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