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Immunologic evidence of a strong association between non-Hodgkin lymphoma and simian virus 40.

Authors :
Tognon M
Luppi M
Corallini A
Taronna A
Barozzi P
Rotondo JC
Comar M
Casali MV
Bovenzi M
D'Agostino A
Vinante F
Rigo A
Ferrarini I
Barbanti-Brodano G
Martini F
Mazzoni E
Source :
Cancer [Cancer] 2015 Aug 01; Vol. 121 (15), pp. 2618-26. Date of Electronic Publication: 2015 Apr 15.
Publication Year :
2015

Abstract

Background: Non-Hodgkin lymphoma (NHL), the most common cancer of the lymphatic system, is of unknown etiology. The identification of etiologic factors in the onset of NHL is a key event that could facilitate the prevention and cure of this malignancy. Simian virus 40 (SV40) has been considered an oncogenic agent in the onset/progression of NHL.<br />Methods: In this study, an indirect enzyme-linked immunosorbent assay with 2 synthetic peptides that mimic SV40 antigens of viral capsid proteins 1 to 3 was employed to detect specific antibodies against SV40. Serum samples were taken from 2 distinct cohorts of NHL-affected patients (NHL1 [n = 89] and NHL2 [n = 61]) along with controls represented by oncologic patients affected by breast cancer (BC; n = 78) and undifferentiated nasopharyngeal carcinoma (UNPC; n = 64) and 3 different cohorts of healthy subjects (HSs; HS1 [n = 130], HS2 [n = 83], and HS3 [n = 87]).<br />Results: Immunologic data indicated that in serum samples from NHL patients, antibodies against SV40 mimotopes were detectable with a prevalence of 40% in NHL1 patients and with a prevalence of 43% in NHL2 patients. In HSs of the same median age as NHL patients, the prevalence was 16% for the HS1 group (57 years) and 14% for the HS2 group (65 years). The difference was statistically significant (P < .0001 and P < .001). Interestingly, the difference between NHL1/NHL2 patients and BC patients (40%/43% vs 15%, P < .001) and between NHL1/NHL2 patients and UNPC patients (40%/43% vs 25%, P < .05) was significant.<br />Conclusions: Our data indicate a strong association between NHL and SV40 and thus a need for innovative therapeutic approaches for this hematologic malignancy.<br /> (© 2015 American Cancer Society.)

Details

Language :
English
ISSN :
1097-0142
Volume :
121
Issue :
15
Database :
MEDLINE
Journal :
Cancer
Publication Type :
Academic Journal
Accession number :
25877010
Full Text :
https://doi.org/10.1002/cncr.29404