Hyposensitizing effect of high altitude and immunogenetic law

The studies were carried out in 24 sexually mature male guinea pigs. They were used as model of immediate-type allergic reaction (active cutaneous anaphylaxis). The animals were divided in 2 groups: control and experimental. The control group was housed in the mountain valley during the study, and the experimental group stayed for 45 days in high mountains (Anzob, 3375 m above sea level). On the day +30, all animals were sensitized with horse serum. On the 12th day of sensitization, blood was taken for analysis, and on the 15th day, an allergic reaction was provoked. We have revealed that, under high-altitude conditions, the severity of reaction was 1.5 times lower than in controls. Moreover, the animals kept in highlands exhibited lower contents of T and B lymphocytes, and IgE antibodies than in the control group. On the contrary, the numbers of phagocytically active neutrophils, as well as total effect of phagocytosis, proved to be higher in this group. This shift may be facilitated by hypoxia, since aerobic processes are known to prevail in the energy metabolism of lymphocytes, and anaerobic processes dominate in neutrophils. The allergic conditions are developed in three stages. Immunological stage is the first and main one, and allergic restructuring of the body immunity largely depends on it. What is the matter of reconstruction under the high-altitude conditions? We suggest, that, along with Haeckel–M ller biogenetic rule, there is also an immunogenetic law: “The activation sequence of events in the body’s defense system is a reproduction of phylogenesis, i.e., switching of subsequent link in defense system follows the evolutionary principles of complication and improvement. Namely, with respect to failing of previous link to completely eliminate the antigen in defense system”. One may conventionally consider that the first protective barrier against antigens is the most evolutionarily ancient structure, i.e., skin and mucous membrane; the second represents factors of nonspecific defense (phagocytosis, lysozyme, interferon, etc.); the third barrier is presented by cellular immunity (T effector cells, etc.), with humoral immunity serving as the fourth barrier. The fifth protective barrier provides evolutionarily late defense, i.e. allergic reaction, which is triggered by Ig E antibodies. On the mentioned basis, one may state that the decreased allergic reaction (the 5th barrier) in the animals from the experimental group was caused by adaptive changes in protective mechanisms of body. One may suggest that, under the high-altitude conditions an increase was observed in functional activity of phagocytes (2nd barrier), along with a decrease in activity of lymphocytes, i.e., cell populations responsible for the evolutionary later protective barriers.

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