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Critical Reviews™ in Immunology

Publicado 6 números por año

ISSN Imprimir: 1040-8401

ISSN En Línea: 2162-6472

The Impact Factor measures the average number of citations received in a particular year by papers published in the journal during the two preceding years. 2017 Journal Citation Reports (Clarivate Analytics, 2018) IF: 1.3 To calculate the five year Impact Factor, citations are counted in 2017 to the previous five years and divided by the source items published in the previous five years. 2017 Journal Citation Reports (Clarivate Analytics, 2018) 5-Year IF: 2.6 The Eigenfactor score, developed by Jevin West and Carl Bergstrom at the University of Washington, is a rating of the total importance of a scientific journal. Journals are rated according to the number of incoming citations, with citations from highly ranked journals weighted to make a larger contribution to the eigenfactor than those from poorly ranked journals. Eigenfactor: 0.00079 The Journal Citation Indicator (JCI) is a single measurement of the field-normalized citation impact of journals in the Web of Science Core Collection across disciplines. The key words here are that the metric is normalized and cross-disciplinary. JCI: 0.24 SJR: 0.429 SNIP: 0.287 CiteScore™:: 2.7 H-Index: 81

Indexed in

Cross-Presentation of Antigens by Dendritic Cells

Volumen 22, Edición 5-6, 2002, 10 pages
DOI: 10.1615/CritRevImmunol.v22.i5-6.50
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SINOPSIS

T lymphocytes recognize antigen presented on the surface of antigen-presenting cells by MHC class I and class II molecules. Classically, MHC class I molecules present self- or pathogen-derived antigens that are synthesized within the cell, whereas exogenous antigens derived via endocytic uptake are loaded onto MHC class II molecules for presentation to CD4+ T cells. It is becoming increasingly clear that some dendritic cells are also specialized to process exogenous antigens into the MHC class I pathway for presentation to CD8+ T cells. This process is known as cross-presentation. It provides a mechanism that can drive dendritic cells to generate either tolerance to self-antigens or immunity to pathogens. The cells responsible for, and mechanisms underlying, this decision between tolerance and immunity via cross-presentation has become the focus of intense study to determine how various dendritic cell subsets effect the different outcomes.

CITADO POR
  1. Aida Virginia, Pliasas Vasilis C., Neasham Peter J., North J. Fletcher, McWhorter Kirklin L., Glover Sheniqua R., Kyriakis Constantinos S., Novel Vaccine Technologies in Veterinary Medicine: A Herald to Human Medicine Vaccines, Frontiers in Veterinary Science, 8, 2021. Crossref

  2. Popella Linda, Steinkasserer Alexander, How Human Herpesviruses Subvert Dendritic Cell Biology and Function, in Innate Immunity in Health and Disease, 2021. Crossref

  3. De Rosa Stephen C., Lu Fabien X., Yu Joanne, Perfetto Stephen P., Falloon Judith, Moser Susan, Evans Thomas G., Koup Richard, Miller Christopher J., Roederer Mario, Vaccination in Humans Generates Broad T Cell Cytokine Responses, The Journal of Immunology, 173, 9, 2004. Crossref

  4. Burgdorf Sven, Lukacs-Kornek Veronika, Kurts Christian, The Mannose Receptor Mediates Uptake of Soluble but Not of Cell-Associated Antigen for Cross-Presentation, The Journal of Immunology, 176, 11, 2006. Crossref

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