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The human cathelicidin hCAP‐18 in serum of children with haemato‐oncological diseases

The human cathelicidin hCAP‐18 (pro‐LL‐37) is the pro‐protein of the antimicrobial peptide LL‐37. hCAP‐18 can be produced by many different cell types; bone marrow neutrophil precursors are the main source of hCAP‐18 in the circulation. Neutrophil count is used as a marker for myelopoiesis but does...

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Autores principales: Jackmann, Natalja, Englund, Sofia, Frisk, Per, Mäkitie, Outi, Utriainen, Pauliina, Mörtberg, Anette, Henriques‐Normark, Birgitta, Pütsep, Katrin, Harila‐Saari, Arja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543647/
https://www.ncbi.nlm.nih.gov/pubmed/35849644
http://dx.doi.org/10.1111/bjh.18360
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author Jackmann, Natalja
Englund, Sofia
Frisk, Per
Mäkitie, Outi
Utriainen, Pauliina
Mörtberg, Anette
Henriques‐Normark, Birgitta
Pütsep, Katrin
Harila‐Saari, Arja
author_facet Jackmann, Natalja
Englund, Sofia
Frisk, Per
Mäkitie, Outi
Utriainen, Pauliina
Mörtberg, Anette
Henriques‐Normark, Birgitta
Pütsep, Katrin
Harila‐Saari, Arja
author_sort Jackmann, Natalja
collection PubMed
description The human cathelicidin hCAP‐18 (pro‐LL‐37) is the pro‐protein of the antimicrobial peptide LL‐37. hCAP‐18 can be produced by many different cell types; bone marrow neutrophil precursors are the main source of hCAP‐18 in the circulation. Neutrophil count is used as a marker for myelopoiesis but does not always reflect neutrophil production in the bone marrow, and thus additional markers are needed. In this study, we established the reference interval of serum hCAP‐18 level in healthy children and compared serum hCAP‐18 levels between different diagnostic groups of children with haemato‐oncological diseases, at diagnosis. We found that children with diseases that impair myelopoiesis, such as acute leukaemia, aplastic anaemia, or myelodysplastic syndrome, presented with low hCAP‐18 levels, whereas patients with non‐haematological malignancies displayed serum hCAP‐18 levels in the same range as healthy children. Children with chronic myeloid leukaemia presented with high circulating levels of hCAP‐18, probably reflecting the high number of all differentiation stages of myeloid cells. We suggest that analysis of serum hCAP‐18 provides additional information regarding myelopoiesis in children with haemato‐oncological diseases, which may have future implications in assessment of myelopoiesis in clinical management.
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spelling pubmed-95436472022-10-14 The human cathelicidin hCAP‐18 in serum of children with haemato‐oncological diseases Jackmann, Natalja Englund, Sofia Frisk, Per Mäkitie, Outi Utriainen, Pauliina Mörtberg, Anette Henriques‐Normark, Birgitta Pütsep, Katrin Harila‐Saari, Arja Br J Haematol Haematological Malignancy–Biology The human cathelicidin hCAP‐18 (pro‐LL‐37) is the pro‐protein of the antimicrobial peptide LL‐37. hCAP‐18 can be produced by many different cell types; bone marrow neutrophil precursors are the main source of hCAP‐18 in the circulation. Neutrophil count is used as a marker for myelopoiesis but does not always reflect neutrophil production in the bone marrow, and thus additional markers are needed. In this study, we established the reference interval of serum hCAP‐18 level in healthy children and compared serum hCAP‐18 levels between different diagnostic groups of children with haemato‐oncological diseases, at diagnosis. We found that children with diseases that impair myelopoiesis, such as acute leukaemia, aplastic anaemia, or myelodysplastic syndrome, presented with low hCAP‐18 levels, whereas patients with non‐haematological malignancies displayed serum hCAP‐18 levels in the same range as healthy children. Children with chronic myeloid leukaemia presented with high circulating levels of hCAP‐18, probably reflecting the high number of all differentiation stages of myeloid cells. We suggest that analysis of serum hCAP‐18 provides additional information regarding myelopoiesis in children with haemato‐oncological diseases, which may have future implications in assessment of myelopoiesis in clinical management. John Wiley and Sons Inc. 2022-07-18 2022-09 /pmc/articles/PMC9543647/ /pubmed/35849644 http://dx.doi.org/10.1111/bjh.18360 Text en © 2022 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Haematological Malignancy–Biology
Jackmann, Natalja
Englund, Sofia
Frisk, Per
Mäkitie, Outi
Utriainen, Pauliina
Mörtberg, Anette
Henriques‐Normark, Birgitta
Pütsep, Katrin
Harila‐Saari, Arja
The human cathelicidin hCAP‐18 in serum of children with haemato‐oncological diseases
title The human cathelicidin hCAP‐18 in serum of children with haemato‐oncological diseases
title_full The human cathelicidin hCAP‐18 in serum of children with haemato‐oncological diseases
title_fullStr The human cathelicidin hCAP‐18 in serum of children with haemato‐oncological diseases
title_full_unstemmed The human cathelicidin hCAP‐18 in serum of children with haemato‐oncological diseases
title_short The human cathelicidin hCAP‐18 in serum of children with haemato‐oncological diseases
title_sort human cathelicidin hcap‐18 in serum of children with haemato‐oncological diseases
topic Haematological Malignancy–Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9543647/
https://www.ncbi.nlm.nih.gov/pubmed/35849644
http://dx.doi.org/10.1111/bjh.18360
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