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Properdin Levels in Individuals with Chemotherapy-Induced Neutropenia

BACKGROUND: Neutrophils produce and carry key components of the alternative pathway (AP) of complement, including properdin (P). The effect of chemotherapy-induced absolute neutropenia on circulating P levels and AP function has not been previously established. METHODS: We prospectively measured fre...

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Autores principales: Tsyrkunou, Artsiom, Agarwal, Sarika, Koirala, Bibek, Finberg, Robert W., Nath, Rajneesh, Barton, Bruce, Levitz, Stuart M., Wang, Jennifer P., Ram, Sanjay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5414105/
https://www.ncbi.nlm.nih.gov/pubmed/28480246
http://dx.doi.org/10.1093/ofid/ofw250
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author Tsyrkunou, Artsiom
Agarwal, Sarika
Koirala, Bibek
Finberg, Robert W.
Nath, Rajneesh
Barton, Bruce
Levitz, Stuart M.
Wang, Jennifer P.
Ram, Sanjay
author_facet Tsyrkunou, Artsiom
Agarwal, Sarika
Koirala, Bibek
Finberg, Robert W.
Nath, Rajneesh
Barton, Bruce
Levitz, Stuart M.
Wang, Jennifer P.
Ram, Sanjay
author_sort Tsyrkunou, Artsiom
collection PubMed
description BACKGROUND: Neutrophils produce and carry key components of the alternative pathway (AP) of complement, including properdin (P). The effect of chemotherapy-induced absolute neutropenia on circulating P levels and AP function has not been previously established. METHODS: We prospectively measured free P levels in serum from 27 individuals expected to develop neutropenia after administration of chemotherapy for hematological malignancies in preparation for hematopoietic stem cell transplantation and here describe the relationship between serum P levels and the neutrophil count over time. RESULTS: When the absolute neutrophil count (ANC) was >500 cells/mm(3) pre-chemotherapy, P levels were significantly higher than P levels associated with an ANC ≤500 cells/mm(3) (median values 8392 ng/mL and 6355 ng/mL, respectively; P = .001). Pairwise comparison between pre-chemotherapy P levels and P levels at initial or last documented neutropenia before recovery showed a significant decline (P < .0001). No correlation was observed between P levels during neutropenia and after recovery of neutropenia in 20 subjects for which postneutropenia samples were obtained. A small but significant (P = .02) decrease in AP hemolytic activity was noted between baseline (preneutropenia) and samples obtained at the onset of neutropenia, but only with low (6.25%) and not higher (12.5 or 25%) serum concentrations. CONCLUSIONS: A decline in P levels and AP activity could contribute to the increased risk of infection in neutropenic patients and warrants further study.
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spelling pubmed-54141052017-05-05 Properdin Levels in Individuals with Chemotherapy-Induced Neutropenia Tsyrkunou, Artsiom Agarwal, Sarika Koirala, Bibek Finberg, Robert W. Nath, Rajneesh Barton, Bruce Levitz, Stuart M. Wang, Jennifer P. Ram, Sanjay Open Forum Infect Dis Major Article BACKGROUND: Neutrophils produce and carry key components of the alternative pathway (AP) of complement, including properdin (P). The effect of chemotherapy-induced absolute neutropenia on circulating P levels and AP function has not been previously established. METHODS: We prospectively measured free P levels in serum from 27 individuals expected to develop neutropenia after administration of chemotherapy for hematological malignancies in preparation for hematopoietic stem cell transplantation and here describe the relationship between serum P levels and the neutrophil count over time. RESULTS: When the absolute neutrophil count (ANC) was >500 cells/mm(3) pre-chemotherapy, P levels were significantly higher than P levels associated with an ANC ≤500 cells/mm(3) (median values 8392 ng/mL and 6355 ng/mL, respectively; P = .001). Pairwise comparison between pre-chemotherapy P levels and P levels at initial or last documented neutropenia before recovery showed a significant decline (P < .0001). No correlation was observed between P levels during neutropenia and after recovery of neutropenia in 20 subjects for which postneutropenia samples were obtained. A small but significant (P = .02) decrease in AP hemolytic activity was noted between baseline (preneutropenia) and samples obtained at the onset of neutropenia, but only with low (6.25%) and not higher (12.5 or 25%) serum concentrations. CONCLUSIONS: A decline in P levels and AP activity could contribute to the increased risk of infection in neutropenic patients and warrants further study. Oxford University Press 2016-12-07 /pmc/articles/PMC5414105/ /pubmed/28480246 http://dx.doi.org/10.1093/ofid/ofw250 Text en © The Author 2016. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com.
spellingShingle Major Article
Tsyrkunou, Artsiom
Agarwal, Sarika
Koirala, Bibek
Finberg, Robert W.
Nath, Rajneesh
Barton, Bruce
Levitz, Stuart M.
Wang, Jennifer P.
Ram, Sanjay
Properdin Levels in Individuals with Chemotherapy-Induced Neutropenia
title Properdin Levels in Individuals with Chemotherapy-Induced Neutropenia
title_full Properdin Levels in Individuals with Chemotherapy-Induced Neutropenia
title_fullStr Properdin Levels in Individuals with Chemotherapy-Induced Neutropenia
title_full_unstemmed Properdin Levels in Individuals with Chemotherapy-Induced Neutropenia
title_short Properdin Levels in Individuals with Chemotherapy-Induced Neutropenia
title_sort properdin levels in individuals with chemotherapy-induced neutropenia
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5414105/
https://www.ncbi.nlm.nih.gov/pubmed/28480246
http://dx.doi.org/10.1093/ofid/ofw250
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