Literature DB >> 17386021

The cross-priming pathway: a portrait of an intricate immune system.

S Basta1, A Alatery.   

Abstract

Antigen presentation by professional antigen-presenting cells (pAPCs) to cytotoxic CD8(+) T cells can occur via two processing routes - the direct and cross-presentation pathways. Cross-presentation of exogenous antigens in the context of major histocompatibility complex (MHC) class I molecules has recently attracted a lot of research interest because it may prove crucial for vaccine development. This alternative pathway has been implicated in priming CD8(+) T-cell responses to pathogens as well as tumours in vivo (cross-priming). In cross-presentation, the internalized antigens can be processed through diverse intracellular routes. As many unresolved questions regarding the molecular basis that controls the cross-priming process still exist, it is essential to explore the various elements involved therein, to better elucidate this pathway. In this review, we summarize current data that explore how the source and nature of antigens could affect their cross-presentation. Moreover, we will discuss and outline how recent advances regarding pAPCs' properties have increased our appreciation of the complex nature of the cross-priming pathway in vivo. In conclusion, we contemplate how the direct and cross-presentation pathways can function to allow the immune system to deal efficiently with diverse pathogens.

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Year:  2007        PMID: 17386021     DOI: 10.1111/j.1365-3083.2007.01909.x

Source DB:  PubMed          Journal:  Scand J Immunol        ISSN: 0300-9475            Impact factor:   3.487


  20 in total

1.  CD8+ T cell immunodominance in lymphocytic choriomeningitis virus infection is modified in the presence of toll-like receptor agonists.

Authors:  Sarah Siddiqui; Sameh Basta
Journal:  J Virol       Date:  2011-09-28       Impact factor: 5.103

2.  TRAIL/DR5 plays a critical role in NK cell-mediated negative regulation of dendritic cell cross-priming of T cells.

Authors:  Mitsuhiro Iyori; Tong Zhang; Haddon Pantel; Bethany A Gagne; Charles L Sentman
Journal:  J Immunol       Date:  2011-08-10       Impact factor: 5.422

3.  HLA-F and MHC-I open conformers cooperate in a MHC-I antigen cross-presentation pathway.

Authors:  Jodie P Goodridge; Ni Lee; Aura Burian; Chul-Woo Pyo; Scott S Tykodi; Edus H Warren; Cassian Yee; Stanley R Riddell; Daniel E Geraghty
Journal:  J Immunol       Date:  2013-07-12       Impact factor: 5.422

Review 4.  MHC and adaptive immunity in teleost fishes.

Authors:  Anthony B Wilson
Journal:  Immunogenetics       Date:  2017-07-10       Impact factor: 2.846

5.  Stable antigen is most effective for eliciting CD8+ T-cell responses after DNA vaccination and infection with recombinant vaccinia virus in vivo.

Authors:  Christopher Schliehe; Annegret Bitzer; Maries van den Broek; Marcus Groettrup
Journal:  J Virol       Date:  2012-07-03       Impact factor: 5.103

6.  Comparative Transcriptomic Immune Responses of Mullet (Mugil cephalus) Infected by Planktonic and Biofilm Lactococcus Garvieae.

Authors:  Feng-Jie Su; Thirunavukkarasu Periyasamy; Meei-Mei Chen
Journal:  Front Cell Infect Microbiol       Date:  2022-05-23       Impact factor: 6.073

7.  Delivery of Exogenous Antigens to Induce Cytotoxic CD8+ T Lymphocyte Responses.

Authors:  Julia Kim; Vandana Gambhir; Attiya Alatery; Sameh Basta
Journal:  J Biomed Biotechnol       Date:  2010-05-23

8.  Alloprimed CD8(+) T cells regulate alloantibody and eliminate alloprimed B cells through perforin- and FasL-dependent mechanisms.

Authors:  J M Zimmerer; T A Pham; C L Wright; K J Tobin; P B Sanghavi; S M Elzein; V M Sanders; G L Bumgardner
Journal:  Am J Transplant       Date:  2014-02       Impact factor: 8.086

9.  Crosspresentation by nonhematopoietic and direct presentation by hematopoietic cells induce central tolerance to myelin basic protein.

Authors:  Antoine Perchellet; Thea Brabb; Joan M Goverman
Journal:  Proc Natl Acad Sci U S A       Date:  2008-09-04       Impact factor: 11.205

10.  Just one position-independent lysine residue can direct MelanA into proteasomal degradation following N-terminal fusion of ubiquitin.

Authors:  Christian Setz; Melanie Friedrich; Sabine Hahn; Jan Dörrie; Niels Schaft; Gerold Schuler; Ulrich Schubert
Journal:  PLoS One       Date:  2013-02-05       Impact factor: 3.240

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