Functional Relevance of Improbable Antibody Mutations for HIV Broadly Neutralizing Antibody Development
Year: 2018
Type: article
Abstract: HIV-1 broadly neutralizing antibodies (bnAbs) require high levels of activation-induced cytidine deaminase (AID)-catalyzed somatic mutations for optimal neutralization potency. Probable mutations occur at sites of frequent AID activity, while improbable mutations occur where AID activity is infrequent. One bottleneck for induction of bnAbs is the evolution of viral envelopes (Envs) that can select bnAb B cell receptors (BCR) with improbable mutations. Here we define the probability of bnAb mutations and demonstrate the functional significance of key improbable mutations in three bnAb B cell lineages. We show that bnAbs are enriched for improbable mutations, which implies that their elicitation will be critical for successful vaccine induction of potent bnAb B cell lineages. We discuss a mutation-guided vaccine strategy for identification of Envs that can select B cells with BCRs that have key improbable mutations required for bnAb development.
Source: Cell Host & Microbe
Institutions: Duke University, Duke Medical Center, Boston University
Language: English
Topic: HIV Research and Treatment
Subfield: Virology
Field: Immunology and Microbiology
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $4,850
Awards: G1770222244, Medical Scientist Training Program, G2724947542, G3056361687, Duke University - to define the protective nature of antibodies that emerge after boosting of the RV144 vaccines, G5267713852, Data commons for 'omic, microscopy and analysis core facilities, G9000127136, Providence/Boston Center for AIDS Research (CFAR), Center for AIDS Research, G926065654
OpenAlex ID: W2805330890
