Premium
Distinct age‐matched serum biomarker profiles in patients with cutaneous T ‐cell lymphoma
Author(s) -
Geskin Larisa J.,
Akilov Oleg E.,
Lin Yan,
Lokshin Anna E.
Publication year - 2014
Publication title -
experimental dermatology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.108
H-Index - 96
eISSN - 1600-0625
pISSN - 0906-6705
DOI - 10.1111/exd.12455
Subject(s) - medicine , immunology , biomarker , immune system , multiplex , eotaxin , cancer , disease , tumor necrosis factor alpha , immunosenescence , chemokine , biology , bioinformatics , biochemistry
Immunological functions decline with age. Because MS /SzS predominately affects the elderly, it is important to distinguish age‐related from cancer‐specific changes. Also, MF and SzS are malignancies of CD 4 + T‐lymphocytes, further compromising an immune state of the patients. The objectives of this study were to distinguish disease‐specific immunological deterioration by performing comparative age ‐ matched Luminex multiplex assessment of 34 serum biomarkers between patients with MF /SzS, HIV‐infected individuals and normal controls. Controlling for age, expression level appears to significantly differ between patients with MF /SzS and controls for the following biomarkers: G‐ CSF , IL ‐5, MIP ‐1 β , TNF ‐ α , VEGF , EOTAXIN , IL ‐8, IL ‐12, IL ‐2R, IP 10, MCP ‐1, MIG , TNFR 1 and TNFR 2 ( P < 0.05), while others showed normal age‐related changes. Interestingly, cluster analysis placed MF /SzS profiles closer to HIV . This further underscores an immunologically compromised state of patients with MF /SzS and suggests its potential self‐perpetuating role in disease progression.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom