TY - JOUR KW - Acquired Immunodeficiency Syndrome KW - Animals KW - Apoptosis KW - Cytokines KW - HIV KW - Humans KW - Hypersensitivity, Immediate KW - Leishmania KW - Liver KW - Mast Cells KW - Mice KW - Models, Biological KW - Murine Acquired Immunodeficiency Syndrome KW - Th1 Cells KW - Th2 Cells KW - Thymic Factor, Circulating KW - Vaccination KW - Virus Replication KW - Zinc AU - Sprietsma J E AB -

Functional, excessive-possibly temporary-deficiencies of the trace element zinc can change immune functions prematurely from predominantly cellular Th1 responses to humoral Th2 responses. T helper (Th1) cells produce cytokines such as interleukin-2 (IL-2) and interferon gamma, thereby controlling viral infections and other intracellular pathogens more effectively than Th2 responses through cytokines such as IL-4, IL-5, IL-6 and IL-10. The accelerated shift from the production of extra Th1 cells during these cellular immune activities to more Th2 cells with their predominantly humoral immune functions, caused by such a zinc deficiency, adversely influences the course of diseases such as leprosy, schistosomiasis, leishmaniasis and AIDS, and can result in allergies. It is noteworthy that AIDS viruses (HIVs) do not replicate in Th1 cells, which probably contain more zinc, but preferentially in the Th0 and Th2 cells; all the more so, because zinc and copper ions are known to inhibit intracellular HIV replication. Considering the above Th1/Th2 switch, real prospects seem to be offered of vaccination against such parasites as Leishmania and against HIVs.

BT - Medical hypotheses C1 - http://www.ncbi.nlm.nih.gov/pubmed/9247900?dopt=Abstract DA - 1997 Jul DO - 10.1016/s0306-9877(97)90244-9 IS - 1 J2 - Med. Hypotheses LA - eng N2 -

Functional, excessive-possibly temporary-deficiencies of the trace element zinc can change immune functions prematurely from predominantly cellular Th1 responses to humoral Th2 responses. T helper (Th1) cells produce cytokines such as interleukin-2 (IL-2) and interferon gamma, thereby controlling viral infections and other intracellular pathogens more effectively than Th2 responses through cytokines such as IL-4, IL-5, IL-6 and IL-10. The accelerated shift from the production of extra Th1 cells during these cellular immune activities to more Th2 cells with their predominantly humoral immune functions, caused by such a zinc deficiency, adversely influences the course of diseases such as leprosy, schistosomiasis, leishmaniasis and AIDS, and can result in allergies. It is noteworthy that AIDS viruses (HIVs) do not replicate in Th1 cells, which probably contain more zinc, but preferentially in the Th0 and Th2 cells; all the more so, because zinc and copper ions are known to inhibit intracellular HIV replication. Considering the above Th1/Th2 switch, real prospects seem to be offered of vaccination against such parasites as Leishmania and against HIVs.

PY - 1997 SP - 1 EP - 14 T2 - Medical hypotheses TI - Zinc-controlled Th1/Th2 switch significantly determines development of diseases. VL - 49 SN - 0306-9877 ER -