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Research Article Free access | 10.1172/JCI107522
Laboratory of Clinical Investigation, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20014
Division of Cancer Treatment, National Cancer Institute, Bethesda, Maryland 20014
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Laboratory of Clinical Investigation, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20014
Division of Cancer Treatment, National Cancer Institute, Bethesda, Maryland 20014
Find articles by Dale, D. in: JCI | PubMed | Google Scholar
Laboratory of Clinical Investigation, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20014
Division of Cancer Treatment, National Cancer Institute, Bethesda, Maryland 20014
Find articles by Omine, M. in: JCI | PubMed | Google Scholar
Laboratory of Clinical Investigation, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20014
Division of Cancer Treatment, National Cancer Institute, Bethesda, Maryland 20014
Find articles by Perry, S. in: JCI | PubMed | Google Scholar
Laboratory of Clinical Investigation, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20014
Division of Cancer Treatment, National Cancer Institute, Bethesda, Maryland 20014
Find articles by Wolff, S. in: JCI | PubMed | Google Scholar
Published December 1, 1973 - More info
Human cyclic neutropenia is characterized by severe depression of blood neutrophil levels approximately every 21 days. To investigate the mechanism of cyclic neutropenia four patients were studied with daily complete blood counts, serial bone marrow examinations, marrow reserve testing, serum muramidase determinations, DF22P granulocytokinetic studies, and, in one patient, in vivo [3H]TdR labeling. Periodogram analysis of the serial blood counts in the latter patient and visual inspection of multiple cycles in the others revealed periodic fluctuations in the levels of blood neutrophils, monocytes, lymphocytes, reticulocytes, and platelets. Rhythmic changes in the morphologic and radioisotopic studies as well as the marrow reserve tests and muramidase measurements were consonant with a mechanism of periodic failure of marrow production rather than peripheral destruction. Human cyclic neutropenia is analogous to cyclic neutropenia in the grey collie dog and may be viewed as the consequence of cyclic hematopoiesis.
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