Literature DB >> 1062227

Specific antigen stimulated lymphocyte proliferation in osteosarcoma.

B J Gainor, J T Forbes, W F Enneking, R T Smith.   

Abstract

A lymphocyte proliferation assay (LPA) for cellular immune responses to osteosarcoma antigens is described and applied to an examination of peripheral blood lymphocytes (PBL) taken from osteosarcoma patients. The antigen preparations were derived from 3 M KC1 solubilized osteosarcoma, taken from a limited number of patients. Lymphocytes from most tumor-bearing patients were stimulated to significant proliferation when cultured in normal human serum. Such stimulation was observed whether or not the lymphoid cells were preincubated 24 hours at 37 degrees C prior to addition of antigen. Patients whose lesion had been resected and who were without evidence of disease for 5-70 months had diminished proliferative responses. Lymphocytes from normal subjects, from patients having other types of sarcoma, and patients having carcinomas rarely responded to the soluble osteosarcoma antigens. When responsive PBL taken from tumor-bearing patients were cultured in autologous serum, the proliferative responses were abrogated or blocked. Serial assays made in the course of bearing this tumor under a variety of therapeutic regimens, including an immunotherapy protocol, suggest that the LPA may be useful in monitoring clinical progress of the disease and possibly in other immunotherapy protocols for osteosarcoma.

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Year:  1976        PMID: 1062227     DOI: 10.1002/1097-0142(197602)37:2<743::aid-cncr2820370222>3.0.co;2-0

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  2 in total

1.  Anti-TGF-β antibody combined with dendritic cells produce antitumor effects in osteosarcoma.

Authors:  Masanori Kawano; Ichiro Itonaga; Tatsuya Iwasaki; Hiroyuki Tsuchiya; Hiroshi Tsumura
Journal:  Clin Orthop Relat Res       Date:  2012-03-14       Impact factor: 4.176

2.  Immune response to chemically induced tumours: correlation of responding cell class with in vivo inhibition of tumour growth.

Authors:  M B Calderwood; J T Forbes; R T Smith
Journal:  Br J Cancer       Date:  1981-04       Impact factor: 7.640

  2 in total

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