Literature DB >> 33229949

COVID-19 antibody development fueled by HIV-1 broadly neutralizing antibody research.

Pilar Mendoza1, Julio C C Lorenzi, Christian Gaebler.   

Abstract

PURPOSE OF REVIEW: The coronavirus disease 2019 (COVID-19) pandemic has caught the world unprepared, with no prevention or treatment strategies in place. In addition to the efforts to develop an effective vaccine, alternative approaches are essential to control this pandemic, which will most likely require multiple readily available solutions. Among them, monoclonal anti-severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) antibodies have been isolated by multiple laboratories in record time facilitated by techniques that were first pioneered for HIV-1 antibody discovery. Here, we summarize how lessons learned from anti-HIV-1 antibody discovery have provided fundamental knowledge for the rapid development of anti-SARS-CoV-2 antibodies. RECENT
FINDINGS: Research laboratories that successfully identified potent broadly neutralizing antibodies against HIV-1 have harnessed their antibody discovery techniques to isolate novel potent anti-SARS-CoV-2 antibodies, which have efficacy in animal models. These antibodies represent promising clinical candidates for treatment or prevention of COVID-19.
SUMMARY: Passive transfer of antibodies is a promising approach when the elicitation of protective immune responses is difficult, as in the case of HIV-1 infection. Antibodies can also play a significant role in post-exposure prophylaxis, in high-risk populations that may not mount robust immune responses after vaccination, and in therapy. We provide a review of the recent approaches used for anti-SARS-CoV-2 antibody discovery and upcoming challenges in the field.

Entities:  

Mesh:

Substances:

Year:  2021        PMID: 33229949     DOI: 10.1097/COH.0000000000000657

Source DB:  PubMed          Journal:  Curr Opin HIV AIDS        ISSN: 1746-630X            Impact factor:   4.283


  2 in total

1.  Preclinical immunological evaluation of an intradermal heterologous vaccine against SARS-CoV-2 variants.

Authors:  Shengtao Fan; Kang Xiao; Dandan Li; Heng Zhao; Jingjing Zhang; Li Yu; Penglan Chang; Shuangli Zhu; Xingli Xu; Yun Liao; Tianjiao Ji; Guorun Jiang; Dongmei Yan; Fengyuan Zeng; Suqin Duan; Baicheng Xia; Lichun Wang; Fengmei Yang; Zhanlong He; Yang Song; Pingfang Cui; Xiaolei Li; Yaxing Zhang; Bangyi Zheng; Ying Zhang; Wenbo Xu; Qihan Li
Journal:  Emerg Microbes Infect       Date:  2022-12       Impact factor: 7.163

2.  Extracellular Loops of the Treponema pallidum FadL Orthologs TP0856 and TP0858 Elicit IgG Antibodies and IgG+-Specific B-Cells in the Rabbit Model of Experimental Syphilis.

Authors:  Kristina N Delgado; Jairo M Montezuma-Rusca; Isabel C Orbe; Melissa J Caimano; Carson J La Vake; Amit Luthra; Christopher M Hennelly; Fredrick N Nindo; Jacob W Meyer; Letitia D Jones; Jonathan B Parr; Juan C Salazar; M Anthony Moody; Justin D Radolf; Kelly L Hawley
Journal:  mBio       Date:  2022-07-12       Impact factor: 7.786

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.