Journal article
T cell-mediated immune response to respiratory coronaviruses
Immunologic research, Vol.59(1-3), pp.118-128
08/2014
DOI: 10.1007/s12026-014-8534-z
PMCID: PMC4125530
PMID: 24845462
Abstract
Emerging respiratory coronaviruses such as the severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome coronavirus (MERS-CoV) pose potential biological threats to humans. SARS and MERS are manifested as severe atypical pneumonia associated with high morbidity and mortality in humans. The majority of studies carried out in SARS-CoV-infected humans and animals attribute a dysregulated/exuberant innate response as a leading contributor to SARS-CoV-mediated pathology. A decade after the 2002-2003 SARS epidemic, we do not have any approved preventive or therapeutic agents available in case of re-emergence of SARS-CoV or other related viruses. A strong neutralizing antibody response generated against the spike (S) glycoprotein of SARS-CoV is completely protective in the susceptible host. However, neutralizing antibody titers and the memory B cell response are short lived in SARS-recovered patients and the antibody will target primary homologous strain. Interestingly, the acute phase of SARS in humans is associated with a severe reduction in the number of T cells in the blood. Surprisingly, only a limited number of studies have explored the role of the T cell-mediated adaptive immune response in respiratory coronavirus pathogenesis. In this review, we discuss the role of anti-virus CD4 and CD8 T cells during respiratory coronavirus infections with a special emphasis on emerging coronaviruses.
Details
- Title: Subtitle
- T cell-mediated immune response to respiratory coronaviruses
- Creators
- Rudragouda Channappanavar - Department of Microbiology, Carver College of Medicine, The University of Iowa, Iowa City, IA, 52242, USAJincun ZhaoStanley Perlman
- Resource Type
- Journal article
- Publication Details
- Immunologic research, Vol.59(1-3), pp.118-128
- DOI
- 10.1007/s12026-014-8534-z
- PMID
- 24845462
- PMCID
- PMC4125530
- NLM abbreviation
- Immunol Res
- ISSN
- 0257-277X
- eISSN
- 1559-0755
- Publisher
- United States
- Grant note
- P01 AI060699 / NIAID NIH HHS R01 AI091322 / NIAID NIH HHS R01 NS036592 / NINDS NIH HHS
- Language
- English
- Electronic publication date
- 05/21/2014
- Date published
- 08/2014
- Academic Unit
- Microbiology and Immunology; Stead Family Department of Pediatrics; Iowa Neuroscience Institute; Infectious Disease (Pediatrics)
- Record Identifier
- 9983777353002771
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