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Biomedical subjects

S I Shereshkov

Publications and source records attributed to S I Shereshkov.

8 recordsLinked to original sources

[Method for the bacteriological study of human embryonic liver cells intended for the treatment of cancer patients].

Native and cryopreserved human embryo liver cells were stored up to be used in cancer patients with antitumor treatment-induced myelodepression. In the course of conservation and before administration, cells were bacteriologically tested after the USSR Ministry of Health standing procedures as well as in some additional serum media. As a result, both classical bacterial forms and their cell wall-degenerate organisms were identified. Contamination of biopreparations with the latter is hazardous for immunodepressive patients.

Bacteriological Techniques

[Hematopoiesis in an organ culture of embryonal human liver].

It was shown by the method of multiple organ cultures on millipore filters that hemopoiesis preferably of erythroid type remained for more than one and a half months in the human embryo liver culture. General morphology of 7--50-day cultures was studied and described. Myeloid population of the cells (CFU conut) was exhausted practically by the 14--16th days of cultivation.

Hematopoiesis

[Cultivation of human peripheral blood leukocytes on agar gel].

It was shown by the modified method of agar cultures that in the peripheral blood of a healthy man, aged from 4 days to 40 years. The number of cell precursors of granulocytes and macrophages (CFU-C) varied from 0.05 to 6.38 in adults and from 0.2 to 2.9 in children per 105 nuclear cells. CFU-C content in the patients with infectious mononucleosis and acute leukemia was 0.5--14 and 0--0.3 per 105 nuclear cells, respectively.

Acute Disease

[Cyclic neutropenia: a disease or a syndrome?].

Peripheral blood and bone marrow morphology, blood and bone marrow lymphocyte subpopulation composition were studied in two children with cyclic neutropenia, using flow cytofluorometry, monoclonal antibodies, colony-forming capacity of granulocytic macrophagal precursors in semi-fluid agar. The studies were conducted in varying periods of the neutropenic cycle. Differences were revealed in immunohematologic parameters and clinical course of neutropenia in the two patients. The analysis of the literature data and the authors' own observations of the patients with cyclic neutropenia permitted a suggestion on high heterogeneity of pathogenetic mechanisms of this disease.

Adolescent