Antibodies reacting with Simian Virus 40 capsid protein mimotopes in serum samples from patients affected by uveal melanoma
- Ilaria Bononi†1,
- Paolo Perri†2,
- Alice Begnardi1,
- Alessandra Martini2,
- Elisa Mazzoni1,
- Silvia Bosi1,
- Silvia Pietrobon1,
- Adolfo Sebastiani2,
- Mauro Tognon2Email author and
- Fernanda Martini2Email author
© Bononi et al.; licensee BioMed Central Ltd. 2014
Received: 19 March 2014
Accepted: 18 April 2014
Published: 29 April 2014
The uveal melanoma (UM) is the most common human intraocular tumour. Simian Virus 40 (SV-40) is a small DNA tumor virus detected in some malignancies, including the cutaneous melanoma. In this study an indirect ELISA using synthetic peptides that mimic SV-40 antigens, was employed to detect antibodies against SV-40 in serum samples from UM patients. Our report indicates a significant higher prevalence of antibodies against SV-40 capsid protein antigens in serum samples from UM patients compared to controls. Our data suggest an association between UM and SV-40, indicating that patients affected by uveal melanoma tested SV-40-positive could be treated by innovative therapies.
KeywordsUveal melanoma Simian Virus 40 ELISA Antibody Prevalence
The uveal melanoma (UM) is the most common primary intraocular tumor. Many studies reported genetic alterations in UM , but the causes are poorly understood. BAP1, a gene encoding a deubiquitinant enzyme, is mutated in several UM cases and in the malignant pleural mesothelioma (MPM) , a human tumour found be associated with the Simian Virus 40 (SV-40) infection [3, 4]. SV-40 oncogenic potential has been demonstrated in experimental animals [3, 4], while its mutagenic activities have been detected in different animal and human cell types [3, 4]. In human tumours, SV-40 was identified for the first time in a patient affected by a cutaneous melanoma , that shares the onset model with UM. Altogether these data were the background that prompted us to investigate the association between UM and SV-40 by analysing the prevalence of SV-40 antibodies in serum samples from UM affected patients. This study was carried out, as reported before, by an indirect Enzyme-Linked Immunosorbent Assay (ELISA) with SV-40 specific synthetic peptides derived from its viral proteins, without cross-reactivity with the closely related BKV and JCV which are obiquitous polyomaviruses in humans .
In this investigation, serum samples from UM affected patients (n = 48) and healthy subjects with ocular nevi (HSON; n = 71) and without ocular nevi (HS; n = 168), with the same median age (66 yrs), were analysed for presence of SV-40 antibodies. All patients and subjects were vaccinated against the poliomyelitis. The immunologic study was carried out by indirect ELISAs employing two specific mimotopes from SV-40 viral capsid proteins 1 and 2–3, named B and C peptides, respectively . In our experiments, serum samples were considered SV-40 VP-positive upon reacting to both peptides B and C. Informed written consent was obtained from the patients and subjects. The study was approved by the County Ethical Committee, Ferrara, Italy.
Our immunologic data indicate that a subset (1/3) of UM is associated with SV-40, a small DNA tumour virus detected as a contaminant in early anti-polio vaccines [3, 4, 7]. At present, SV-40 infection seems to spread in humans by different ways, including the urine and the faecal-oral route [3, 4, 7].
UM onset, like other human cancers, is due to specific gene mutations. Since SV-40 is oncogenic, clastogenic, mutagenic and a transforming viral agent [3, 7], may be a risk factor, together with other oncogenic agents such as the U.V. irradiation, in the UM onset/progression . One may postulate that after infecting the host, SV-40 may exert its tumourigenic potential when the immune system is impaired. The high prevalence of SV-40 antibodies in sera from UM affected patients is not proof of cause/effect in inducing human tumours by SV-40. SV-40 DNA and expression of its oncogene, the large T antigen, should be analysed in UM specimens to confirm and extend the potential role of this oncogenic virus in UM onset/progression. We should also consider, as an alternative explanation, that another not yet discovered human Polyomavirus closely related to SV-40 may be responsible of our immunologic data. Our results from the laboratory bench could be transferred to the clinical application employing specific innovative therapies for SV40-positive UM patients.
Dr. Elisa Mazzoni is a post doctoral fellow of the Fondazione Veronesi, Milan, Italy.
We would like to thank Dr. Eugene O. Major, the Laboratory of Molecular Medicine and Neuroscience, the National Institute of Neurological Disorders and Stroke, Bethesda, MD, for the hyperimmmune serum against JCV.
Supported, in part, by grants from University of Ferrara, FAR projects, Ferrara and PRIN 2008, from MIUR, Rome. Italy. All authors actively contributed to this work.
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