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After nearly four decades of research, a safe and effective HIV-1 vaccine remains elusive. There are many reasons why the development of a potent and durable HIV-1 vaccine is challenging, including the extraordinary genetic diversity of HIV-1 and its complex mechanisms of immune evasion. HIV-1 envelope glycoproteins are poorly recognized by the immune system, which means that potent broadly neutralizing antibodies (bnAbs) are only infrequently induced in the setting of HIV-1 infection or through vaccination. Thus, the biology of HIV-1-host interactions necessitates novel strategies for vaccine development to be designed to activate and expand rare bnAb-producing B cell lineages and to select for the acquisition of critical improbable bnAb mutations. Here we discuss strategies for the induction of potent and broad HIV-1 bnAbs and outline the steps that may be necessary for ultimate success.

Original publication

DOI

10.1038/s41577-022-00753-w

Type

Journal article

Journal

Nature reviews. Immunology

Publication Date

03/2023

Volume

23

Pages

142 - 158

Addresses

Duke Human Vaccine Institute, Duke University School of Medicine, Durham, NC, USA. barton.haynes@duke.edu.

Keywords

Humans, HIV-1, HIV Infections, AIDS Vaccines, HIV Antibodies, Antigens, Viral, Antibodies, Neutralizing, Broadly Neutralizing Antibodies