Active Crohn's Disease Patients Show a Distinctive Expansion of Circulating Memory CD4+CD45RO+CD28null T Cells
Abstract
In a previous study we found an expansion of circulating memory (CD45RO(+)) CD4(+) T cells in patients with Crohn's disease (CD). The aim of this work was to investigate the phenotypic and functional characteristics of this T-cell subset in CD. We analyzed in peripheral blood CD4(+)CD45RO(+) T cells from CD patients the expression of surface markers associated to immune activation, costimulation, and apoptosis. In sorted CD4(+)CD45RO(+) T cells apoptosis was quantified by fluorescent annexin V binding. Healthy subjects and patients with ulcerative colitis and acute bacterial enterocolitis served as control groups. An increased percentage of memory CD4(+)CD45RO(+) T cells lacking the expression of costimulatory receptor CD28 was detected in patients with active CD when compared to the other groups evaluated. This expanded CD4(+)CD45RO(+)CD28(null) T-cell subset expressed mostly the effector-cell marker CD57(+). Both CD28 downregulation and CD57 expression correlated to CDAI and surrogate markers of disease activity. These phenotypic changes observed on CD4(+)CD45RO(+) T cells from active CD returned to values similar to healthy controls after clinical remission. Moreover, this memory CD28(null) T-cell subset might express more intracytoplasmic TNF and IFN-gamma than their CD28(+) counterpart. Significantly lower frequencies of memory CD4(+)CD45RO(+) T cells expressing CD95 apoptosis receptor were found in patients with active CD. Moreover, sorted CD4(+)CD45RO(+)and CD4(+)CD45R…
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CD28-negative effector memory CD4+ T-cells have been reported in humans only in association with autoimmune diseases such as rheumatoid arthritis, Crohn's disease or multiple sclerosis.
“Effector memory CD4 + T-cells lacking CD28 expression have been reported in humans, but only in association with autoimmune diseases such as rheumatoid arthritis, Crohn's disease or multiple sclerosis (Markovic-Plese et al., 2001;Fasth et al., 2004;Garcia de Tena et al., 2004), and were not observed with the healthy donors used in this study.”
From Monoclonal antibody TGN1412 trial failure explained by species differences in CD28 expression on CD4 <sup>+</sup> effector memory T‐cells (2010) · cites this paper as Garcia de Tena et al., 2004
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“Moreover, they display an increased production of proinflammatory cytokines (33, 36‐38) as well as cytotoxic capacity (37, 39, 40 ) raising the hypothesis that the expansion of CD4 C CD28 null T cells found in such diseases may have a pathogenic role in the development of these disorders (31, 35).”
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- Authors
- De Tena, J. G., Manzano, L., Leal, J. C., Antonio, E. S., Sualdea, V., & Álvarez-Mon, M.
- Affiliations
- Hospital Universitario Príncipe de Asturias (ES)
- ORCID
- Antonio, Esther San
- Venue
- Journal of Clinical Immunology
- Published
- 2004-03
- Volume
- 24
- Issue
- 2
- Pages
- 185-196
- ISSN
- 0271-9142 (ISSN-L)
- 1573-2592
- OpenAlex
- W2031601446
- Cited by
- 59
- References
- 5
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 4 · 2023: 1 · 2022: 2 · 2021: 1 · 2020: 3 · 2019: 4 · 2018: 3 · 2017: 3 · 2016: 3 · 2015: 2 · 2014: 3 · 2013: 3 · 2012: 1
- FWCI
- 1.78
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- Locations
- Journal of Clinical Immunology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Inflammatory Bowel Disease
- Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
- Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
- Keywords
- Crohn's disease, memory CD4+ T cells, CD45RO, CD57, apoptosis resistance, Fas, TNF-α, interferon-gamma, disease activity, clinical remission, ulcerative colitis, T cell costimulation
- MeSH terms
- Adult, Crohn Disease, Female, Humans, Immunologic Memory, Male, CD4-Positive T-Lymphocytes, Cytokines, Apoptosis, Leukocyte Common Antigens, CD28 Antigens
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