Publications by authors named "Jefferson Driscoll"

Introduction: The paucity of objective data on the residency application is challenging to Orthopedic Surgery residency programs when selecting candidates to interview and to rank. Qualifying or quantifying the effect of geography on match results will help programs screen and rank candidates more effectively. The aim of this study is to describe the geographic background of current Orthopedic Surgery residents in the United States relative to their current residency program.

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Antibodies that target the gp120-gp41 interface of the HIV-1 envelope (Env) trimer comprise a commonly elicited category of broadly neutralizing antibodies (bNAbs). Here, we isolate and characterize VRC44, a bNAb lineage with up to 52% neutralization breadth. The cryoelectron microscopy (cryo-EM) structure of antibody VRC44.

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The isolation and characterization of neutralizing antibodies from infection and vaccine settings informs future vaccine design, and methodologies that streamline the isolation of antibodies and the generation of B cell clones are of great interest. Retroviral transduction to express Bcl-6 and Bcl-xL and transform primary B cells has been shown to promote long-term B cell survival and antibody secretion , and can be used to isolate antibodies from memory B cells. However, application of this methodology to B cell subsets from different tissues and B cells from chronically infected individuals has not been well characterized.

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Article Synopsis
  • The HIV-1 envelope trimer (Env) is dynamic and exists in multiple conformational states, crucial for how broadly neutralizing antibodies (bnAbs) target and block the virus's entry into cells.
  • Research using single-molecule Förster resonance energy transfer (smFRET) has identified at least three states of Env, with most bnAbs recognizing a prevalent State 1 prior to the trimer engaging with host receptors.
  • The study found significant differences in the binding of bnAbs to Env in different states, suggesting that the structural differences between State 1 and State 3 are substantial, providing key insights into the otherwise unknown structure of Env in State 1.
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Lineage-based vaccine design is an attractive approach for eliciting broadly neutralizing antibodies (bNAbs) against HIV-1. However, most bNAb lineages studied to date have features indicative of unusual recombination and/or development. From an individual in the prospective RV217 cohort, we identified three lineages of bNAbs targeting the membrane-proximal external region (MPER) of the HIV-1 envelope.

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