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Dead tumor cells improve melanoma vaccine immunogenicity.

Vaccine Weekly

| October 16, 2002 | COPYRIGHT 2002 NewsRX. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

2002 OCT 16 - (NewsRx.com & NewsRx.net) -- by Maria G. Essig, MS, ELS, senior medical writer - A higher number of dead tumor cells in a vaccine containing autologous melanoma tumor cells increased the delayed-type hypersensitivity response in melanoma patients, according to investigators in the U.S.

"We have reported that treatment of melanoma patients with a vaccine consisting of autologous tumor cells modified with the hapten, dinitrophenyl (DNP) and preceded by low-dose cyclophosphamide induces delayed-type hypersensitivity (DTH) to autologous, unmodified tumor cells and that this response is a significant predictor of survival," said David Berd and colleagues at Thomas Jefferson University in Philadelphia.

The investigators examined the characteristics of melanoma vaccines administered to 284 patients who had undergone surgery for malignant melanoma. After vaccination, 161 (57%) of the patients exhibited a DTH reaction of at least 5 mm induration to unmodified autologous tumor cells. No association was found between the number of live melanoma cells in a vaccine dose and the extent of the DTH response (Effect of the dose and composition of an analogous hapten-modified melanoma vaccine on the development of delayed-type hypersensitivity responses. Cancer Immunology Immunotherapy, 2002;51(6):320-326).

However, a significant association was found between the average percentage of dead melanoma cells in the vaccines given to a patient and that patient's maximum DTH response. Sixty-five percent of patients who received vaccines averaging greater than 75% dead cells had ...

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Source: HighBeam Research, Dead tumor cells improve melanoma vaccine immunogenicity.

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