CD8 T cells and E-cadherin in host responses against oropharyngeal candidiasis
- K. Quimby,
- E. A. Lilly,
- M. Zacharek,
- K. McNulty,
- J. E. Leigh,
- Louisiana State University Health Sciences Center,
- Louisiana State University Health Sciences,
- Henry Ford Health System
Open access
Sustainable Development Goals
- SDG 3 Good Health and Well
Abstract
Background: Oropharyngeal candidiasis (OPC) is the most common oral infection in HIV+ persons. Previous studies suggest a role for CD8+ T cells against OPC when CD4+ T cells are lost, but enhanced susceptibility to infection occurs when CD8+ T-cell migration is inhibited by reduced tissue E-cadherin. Objective: To conduct a longitudinal study of tissue CD8+ T-cells and E-cadherin expression before, during, and after the episodes of OPC. Methods: Oral fungal burden was monitored and tissue was evaluated for CD8+ T cells and E-cadherin over a 1-year period in HIV+ persons with a history of, or an acute episode of, OPC. Results: While longitudinal analyses precluded formal interpretations, point prevalence analyses of the data set revealed that when patients experiencing OPC were successfully treated, tissue E-cadherin expression was similar to that in patients who had not experienced OPC, and higher numbers of CD8+ T cells were distributed throughout OPC- tissue under normal expression of E-cadherin. Conclusion: These results suggest that (1) reduction in tissue E-cadherin expression in patients with OPC+ is not permanent, and (2) high numbers of CD8+ T cells can be distributed throughout OPC- tissue under normal E-cadherin expression. Together, these results extend our previous studies and continue to support a role for CD8+ T cells in host defense against OPC.
Publication Information
Output type
Original language
English (US)Pages from-to (Number of pages)
Pages 153-161 (9 pages)Journal (Volume, Issue Number)
Oral Diseases (Volume 18, Issue 2)Publication milestones
- Published - 03/2012
Publication status
ISSN
1354-523XPublication IDs
- Scopus: 84855957132
- PubMed: 21958417
- ORCID: /0000-0001-5774-819X/work/227133051
