HIV-1 hijacks the cell extracellular matrix to spread collectively and efficiently between T lymphocytes
Inizan, C.; Caillet, M.; Desrames, A.; Bomme, P.; MALLET, A.; Bourdic, K.; Lambotte, O.; Boufassa, F.; Mesel-Lemoine, M.; Tangy, F.; Pancino, G.; Mouquet, H.; Lagache, t.; Dufour, A. C.; Olivo-Marin, J.-C.; Rey, F. A.; Saez-Cirion, A.; Thoulouze, M.-I.
Show abstract
Collective transmission via structures containing several virions has recently emerged as a highly efficient mode of viral spread. Here, we demonstrate that HIV-1 spreads between T lymphocytes in the form of viral particles colonies that are concentrated and sheltered in an extracellular matrix (ECM) lattice enabling their collective transmission upon cell contacts. Intrinsically, ECM-clustered viruses infect T lymphocytes more efficiently than individual viral particles. They preserve HIV-1 transmission from antiretroviral treatment (ArT) and potent broadly neutralizing antibodies. We also show that collagen induced by HIV-1 infection controls the clustering of virions and their collective spread, thereby enhancing infectivity. CD4+ T cells from HIV-1-infected patients produce and transmit ECM-virus clusters, supporting that they could be involved in vivo. This study provides new insights into modes of HIV-1 transmission and identifies a novel fundamental role for collagen in this process. HIV-1 spread via ECM-virus clusters may have important implications for viral dissemination and persistence, including during therapy.
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