TY - JOUR
T1 - Analysis of T‐cell‐receptor variable gene segment usage in peripheral‐blood lymphocytes of advanced cancer patients
AU - Angevin, Eric
AU - Farace, Françoise
AU - Genevée, Catherine
AU - Caignard, Anne
AU - Dietrich, Pierre‐Yves ‐Y
AU - Hercend, Thierry
AU - Triebel, Frédéric
AU - Henry‐Amar, Michel
AU - Escudier, Bernard
PY - 1993/1/1
Y1 - 1993/1/1
N2 - Advanced cancer patients generally display impaired T‐cell immune functions. The underlying mechanisms are not well understood. The aim of this study was to analyze whether major alterations of TCR variable gene segment usage could be detected in the blood of these patients. Seventeen individuals with various malignancies were tested using PCR and a panel of V‐gene‐segment‐sub‐family‐specific (Vα1‐w29/Vβ1‐w24) oligonucleotide primers. The results indicate that these cancer patient lymphocytes expressed most Vα and Vβ sub‐family specificities, similarly to the lymphocytes of healthy donors (n = 10). This suggests that immunodepression in advanced cancer patients is not related to major deletions in their T‐cell repertoires. We also compared the mean relative expression of each V‐sub‐family specificity of patients and healthy donors by quantitative densitometric analysis. We found significant differences in 4 Vβ specificities (and no Vα). Our analysis identified unique T‐cell sub‐sets putatively involved in the mechanisms leading to immunodepression in advanced cancer patients. Alternatively, the observed differences in terms of Vβ specificity expression may reflect the host response against the tumor.
AB - Advanced cancer patients generally display impaired T‐cell immune functions. The underlying mechanisms are not well understood. The aim of this study was to analyze whether major alterations of TCR variable gene segment usage could be detected in the blood of these patients. Seventeen individuals with various malignancies were tested using PCR and a panel of V‐gene‐segment‐sub‐family‐specific (Vα1‐w29/Vβ1‐w24) oligonucleotide primers. The results indicate that these cancer patient lymphocytes expressed most Vα and Vβ sub‐family specificities, similarly to the lymphocytes of healthy donors (n = 10). This suggests that immunodepression in advanced cancer patients is not related to major deletions in their T‐cell repertoires. We also compared the mean relative expression of each V‐sub‐family specificity of patients and healthy donors by quantitative densitometric analysis. We found significant differences in 4 Vβ specificities (and no Vα). Our analysis identified unique T‐cell sub‐sets putatively involved in the mechanisms leading to immunodepression in advanced cancer patients. Alternatively, the observed differences in terms of Vβ specificity expression may reflect the host response against the tumor.
UR - http://www.scopus.com/inward/record.url?scp=0027232049&partnerID=8YFLogxK
U2 - 10.1002/ijc.2910540111
DO - 10.1002/ijc.2910540111
M3 - Article
C2 - 8478148
AN - SCOPUS:0027232049
SN - 0020-7136
VL - 54
SP - 60
EP - 67
JO - International Journal of Cancer
JF - International Journal of Cancer
IS - 1
ER -