sCD30, Bcl-2 and anti-annexin V antibodies - apoptosis associated soluble molecules in atopic subjects

S. Zeglen, B. Rogala (Zabrze, Poland)

Source: Annual Congress 2002 - Cellular reactions in allergy in humans and animals
Session: Cellular reactions in allergy in humans and animals
Session type: Poster Discussion
Number: 304
Disease area: Airway diseases

Congress or journal article abstract

Abstract

Bacground: The intensified CD30 expression is associated with the apoptosis pathway of human Th-2 type cells. The CD30 mediated apoptosis is thought to be inhibited by Bcl-2.
Aim: The sCD30 (plasma) and Bcl-2 (lymphocytes lysates, ex vivo) concentrations were estimated and compared with unspecific serum apoptosis marker – anti-Annexin V antibodies.
Methods: 21 atopic subjects (AT, 12 men and 9 women, mean age-28,1) with seasonal allergic rhinitis and episodic asthma symptoms, sensitive to grass pollens, were included into the trial. Control group (C) consisted of 15 healthy donors. The enzyme immunoassay (CD30 DAKO, Bcl-2 ELISA and anti-Annexin V Bender MedSystem) for soluble CD30 (plasma), Bcl-2 (lysates of isolated lymphocytes, ex vivo) and anti-Annexin V antibodies (serum) were used.
Results: The Bcl-2 and anti-Annexin V antibodies concentrations were comparable in atopic and control groups (Bcl-2 mean ±] SEM: AT - 348 ±] 21 pg/mL vs C - 317 ±] 33 pg/mL, anti-Annexin V mean ±] SEM: AT - 2,4 ±] 1,34 U/mL vs C - 1,6 ±] 0,39 U/mL, p>0,05 test U Mann-Whitney). The sCD30 concentration was significantly increased in atopic patients (sCD30 mean ±] SEM: AT - 31,74 ±] 7,3 U/mL vs C - 10,9 ±] 1,4 U/mL; p<0,05 test U Mann-Whitney). Moderate correlation between CD30 and anti-Annexin antibodies was observed (r = -0,48, p<0,05; Spearman test).
Conclusion: Apoptosis of Th-2 type lymphocytes seems to be suppressed in a different than Bcl-2-regulated pathway in atopic patients.


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S. Zeglen, B. Rogala (Zabrze, Poland). sCD30, Bcl-2 and anti-annexin V antibodies - apoptosis associated soluble molecules in atopic subjects. Eur Respir J 2002; 20: Suppl. 38, 304

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