Protection or damage: a dual role for the virus-specific cytotoxic T lymphocyte response in hepatitis B and C infection?
Current Opinion in Immunology, ISSN: 0952-7915, Vol: 12, Issue: 4, Page: 403-408
2000
- 97Citations
- 23Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations97
- Citation Indexes97
- 97
- CrossRef81
- Captures23
- Readers23
- 23
Review Description
During infection with hepatitis B or C viruses, cytotoxic T lymphocytes (CTLs) have been implicated as both the mediators of protection and the principal effectors of liver pathology. Recent studies have allowed an investigation of the relationship between virus-specific CTL responses, liver damage and viral replication. In the presence of an efficient virus-specific CTL response, a scenario is emerging where inhibition of viral replication can be independent of liver pathology. We discuss the possibility that an inadequate CTL response — unable to control viral replication — may contribute to liver pathology not only directly but also via the recruitment of non-virus-specific T cells.
Bibliographic Details
http://www.sciencedirect.com/science/article/pii/S0952791500001084; http://dx.doi.org/10.1016/s0952-7915(00)00108-4; http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=0034126609&origin=inward; http://www.ncbi.nlm.nih.gov/pubmed/10899021; https://linkinghub.elsevier.com/retrieve/pii/S0952791500001084; http://dx.doi.org/10.1016/s0952-7915%2800%2900108-4; https://dx.doi.org/10.1016/s0952-7915%2800%2900108-4
Elsevier BV
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