Abstract |
Accumulating data are showing that the humoral immune response against tumors could favor tumor progression. However, no B lymphocyte pathology has been reported in cancer. Using anti-IgM Ab we nonspecifically depleted B cells in tumor-bearing mice, a treatment that resulted in significant reduction of tumor burden. We analyzed the B lymphocyte phenotype of abdominal lymph nodes and peripheral blood from advanced colon cancer patients by flow cytometry, and compared the B cell phenotype with that found in samples from normal donors. In both lymph nodes and peripheral blood of cancer patients, abnormal populations of B lymphocytes appeared that express an increased CD21 and/or sTn antigens on their cell surface. All patients showed a reduction of CD19+ cells. In a limited clinical test, we analyzed the effects of a partial B cell depletion with Rituximab. The treated patients did not develop any side-effects; the CD21-hyperpositive lymphocytes were reduced, but the proportion of sTn-positive lymphocytes remained unaffected. Apparent reduction of the tumor burden was reported in 50% of the patients when the treatment was ended.
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Authors | E Barbera-Guillem, M B Nelson, B Barr, J K Nyhus, K F May Jr, L Feng, J W Sampsel |
Journal | Cancer immunology, immunotherapy : CII
(Cancer Immunol Immunother)
Vol. 48
Issue 10
Pg. 541-9
(Jan 2000)
ISSN: 0340-7004 [Print] Germany |
PMID | 10630306
(Publication Type: Journal Article)
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Chemical References |
- Antibodies, Monoclonal
- Antibodies, Monoclonal, Murine-Derived
- Antibodies, Neoplasm
- Antigen-Antibody Complex
- Antigens, Neoplasm
- Rituximab
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Topics |
- Animals
- Antibodies, Monoclonal
(therapeutic use)
- Antibodies, Monoclonal, Murine-Derived
- Antibodies, Neoplasm
(blood)
- Antigen-Antibody Complex
(blood)
- Antigens, Neoplasm
(immunology)
- B-Lymphocytes
(pathology)
- Colorectal Neoplasms
(immunology, therapy)
- Female
- Humans
- Lymph Nodes
(pathology)
- Lymphocyte Depletion
- Mammary Neoplasms, Animal
- Melanoma, Experimental
- Mice
- Phenotype
- Rituximab
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