Background
CD4+CD25+ regulatory T cells (Treg), which constitute about 2–3% of CD4+ human T cells, are the main contributors to the maintenance of immune tolerance. Cancer patients, including Melanoma patients bear increased number of circulating and tumor infiltrating Treg that exert functional inhibition on tumor-specific T cells.
Temozolomide (sometimes referred to as TMZ) is an imidazotetrazine derivative of the alkylating agent dacarbazine.
Immunological factors relating to the antitumor effect of temozolomide ... appeared to suppress the frequency of CD4(+) CD25(+) regulatory T cells (Treg).
So base on the research, if activation occurs (mmune activation induced by the HD IL-2) IL-2 being a growth factor for the T-cells, will help fuel their expansion. Since the Tregs are a subset of the CD4+ T-cells, they too will proliferate.
By adding TMZ to the protocol, it suppresses the Treg function and shifts the balance tolerance toward activation of an immune response.
See the abstract at the ASCO Symposium 2010 "Ability of unsuccessful high-dose IL-2 therapy followed immediately by low-dose metronomic temozolomide to induce complete and near-complete remissions in metastatic melanoma."
Source:http://www.abstract.asco.org/AbstView_74_41534.html


“It is not the strongest of the species that survives, nor the most intelligent, but the one most responsive to change.”
~Charles Darwin~
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Jimmy B

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