Cd34t+ humanized mouse model to study mucosal hiv-1 transmission and prevention

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Abstract

Humanized mice are critical for HIV-1 research, but humanized mice generated from cord blood are inefficient at mucosal HIV-1 transmission. Most mucosal HIV-1 transmission studies in mice require fetal tissue-engraftment, the use of which is highly restricted or prohibited. We present a fetal tissue-independent model called CD34T+ with enhanced human leukocyte levels in the blood and improved T cell homing to the gut-associated lymphoid tissue. CD34T+ mice are highly permissive to intra-rectal HIV-1 infection and also show normal env diversification in vivo despite high viral replication. Moreover, mucosal infection in CD34T+ mice can be prevented by infusion of broadly neutralizing antibodies. CD34T+ mice can be rapidly and easily generated using only cord blood cells and do not require any complicated surgical procedures for the humanization process. Therefore, CD34T+ mice provide a novel platform for mucosal HIV-1 transmission studies as well as rapid in vivo testing of novel prevention molecules against HIV-1.

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Vanshylla, K., Held, K., Eser, T. M., Gruell, H., Kleipass, F., Stumpf, R., … Klein, F. (2021). Cd34t+ humanized mouse model to study mucosal hiv-1 transmission and prevention. Vaccines, 9(3), 1–16. https://doi.org/10.3390/vaccines9030198

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