4.6 Review

Antibody class-switching as a strategy to improve HIV-1 neutralization

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TRENDS IN MOLECULAR MEDICINE
卷 28, 期 11, 页码 979-988

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ELSEVIER SCI LTD
DOI: 10.1016/j.molmed.2022.08.010

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资金

  1. National Institute of Allergy and Infectious Diseases of the National Institutes of Health [U01AI136677]
  2. South African Research Chairs Initiative of the Department of Science and Innovation (DSI)
  3. National Research Foundation (NRF) [98341]
  4. South African Medical Research Council SHIP program
  5. Centre for the AIDS program of research (CAPRISA)
  6. Poliomyelitis Research Foundation
  7. Columbia University-Southern African Fogarty AIDS International Training and Research Program (AITRP)

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In this review, the significance of different antibody isotypes for HIV-1 neutralization breadth and potency is discussed, along with how this knowledge can be utilized to enhance passive and active immunization against HIV-1.
Broadly neutralizing antibodies (bNAbs), when administered through passive immunization, are protective against HIV-1 infection. Current HIV-1 vaccine strate-gies are aimed at guiding the immune system to make bNAbs by mimicking their development during infection. Somatic hypermutation of the variable region is known to be crucial for the development of bNAbs. More recently, however, studies have shown how class-switch recombination (CSR) resulting in the generation of different antibody isotypes may serve as an additional mechanism through which antibodies can gain neutralization breadth and potency. In this review, we discuss the importance of different antibody isotypes for HIV-1 neutralization breadth and potency and how this information can be leveraged to improve passive and active immunization against HIV-1.

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