F
Francis R. Carbone
Researcher at University of Melbourne
Publications - 216
Citations - 37352
Francis R. Carbone is an academic researcher from University of Melbourne. The author has contributed to research in topics: Cytotoxic T cell & T cell. The author has an hindex of 83, co-authored 213 publications receiving 35098 citations. Previous affiliations of Francis R. Carbone include Cooperative Research Centre & Washington University in St. Louis.
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Journal ArticleDOI
Electroporation and commercial liposomes efficiently deliver soluble protein into the MHC class I presentation pathway. Priming in vitro and in vivo for class I-restricted recognition of soluble antigen.
TL;DR: Delivery of soluble OVA by both electroporation and commercial liposomes proved more efficient than osmotic loading in sensitising for class I presentation and provides a simple and efficient way of studying class I-restricted T cell recognition of soluble protein antigens.
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Blood-stage Plasmodium berghei infection leads to short-lived parasite-associated antigen presentation by dendritic cells.
Rachel J. Lundie,Rachel J. Lundie,Louise J. Young,Gayle M. Davey,Gayle M. Davey,Jose A Villadangos,Jose A Villadangos,Francis R. Carbone,William R. Heath,William R. Heath,William R. Heath,Brendan S. Crabb,Brendan S. Crabb,Brendan S. Crabb +13 more
TL;DR: It is shown that while P. berghei‐expressed antigens were presented early in infection, there was a rapid decline in presentation within 4 days, paralleling impairment in MHC class I‐ and II‐restricted presentation of third party antIGens, providing important evidence that P.berghei not only causes immunosuppression to subsequently encountered third partyAntigens, but also rapidly limits the capacity to generate effective parasite‐specific immunity.
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Antigen-specific CD8+ T cell subset distribution in lymph nodes draining the site of herpes simplex virus infection.
TL;DR: Although lymph node CD8+ T cell numbers increase as a consequence of HSV infection, the majority of these cells are small resting cells that are not enriched for gB‐specific receptors, which is consistent with a nonspecific migration of CTL precursors into the lymph nodes draining the site of infection.
Journal ArticleDOI
Immunology: dangerous liaisons.
TL;DR: Uric acid released by damaged cells is a danger signal that is able to notify immune cells of microbial attack and alert the immune system to invading microorganisms.
Journal ArticleDOI
Blood-Stage Plasmodium berghei Infection Generates a Potent, Specific CD8+ T-Cell Response Despite Residence Largely in Cells Lacking MHC I Processing Machinery
Lei Shong Lau,Daniel Fernandez Ruiz,Gayle M. Davey,Gayle M. Davey,Tania F. de Koning-Ward,Anthony T. Papenfuss,Francis R. Carbone,Andrew G. Brooks,Brendan S. Crabb,Brendan S. Crabb,Brendan S. Crabb,William R. Heath,William R. Heath +12 more
TL;DR: It is indicated that vigorous CTL responses can be induced to pathogens even when they largely reside in red blood cells, which lack MHC I processing machinery.