Chemotherapeutic treatment reduces circulating levels of surfactant protein-D in children with acute lymphoblastic leukemia

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Chemotherapeutic treatment reduces circulating levels of surfactant protein-D in children with acute lymphoblastic leukemia. / Rathe, Mathias; Sorensen, Grith L.; Wehner, Peder S.; Holmskov, Uffe; Sangild, Per T.; Schmiegelow, Kjeld; Müller, Klaus; Husby, Steffen.

In: Pediatric Blood & Cancer, Vol. 64, No. 3, e26253 , 2017.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Rathe, M, Sorensen, GL, Wehner, PS, Holmskov, U, Sangild, PT, Schmiegelow, K, Müller, K & Husby, S 2017, 'Chemotherapeutic treatment reduces circulating levels of surfactant protein-D in children with acute lymphoblastic leukemia', Pediatric Blood & Cancer, vol. 64, no. 3, e26253 . https://doi.org/10.1002/pbc.26253

APA

Rathe, M., Sorensen, G. L., Wehner, P. S., Holmskov, U., Sangild, P. T., Schmiegelow, K., Müller, K., & Husby, S. (2017). Chemotherapeutic treatment reduces circulating levels of surfactant protein-D in children with acute lymphoblastic leukemia. Pediatric Blood & Cancer, 64(3), [e26253 ]. https://doi.org/10.1002/pbc.26253

Vancouver

Rathe M, Sorensen GL, Wehner PS, Holmskov U, Sangild PT, Schmiegelow K et al. Chemotherapeutic treatment reduces circulating levels of surfactant protein-D in children with acute lymphoblastic leukemia. Pediatric Blood & Cancer. 2017;64(3). e26253 . https://doi.org/10.1002/pbc.26253

Author

Rathe, Mathias ; Sorensen, Grith L. ; Wehner, Peder S. ; Holmskov, Uffe ; Sangild, Per T. ; Schmiegelow, Kjeld ; Müller, Klaus ; Husby, Steffen. / Chemotherapeutic treatment reduces circulating levels of surfactant protein-D in children with acute lymphoblastic leukemia. In: Pediatric Blood & Cancer. 2017 ; Vol. 64, No. 3.

Bibtex

@article{5b63fd27fb7644568780aab5f82d09d6,
title = "Chemotherapeutic treatment reduces circulating levels of surfactant protein-D in children with acute lymphoblastic leukemia",
abstract = "BACKGROUND: Surfactant protein D (SP-D) is a host defense molecule of the innate immune system that enhances pathogen clearance and modulates inflammatory responses. We hypothesized that circulating SP-D levels are associated with chemotherapy-induced mucositis and infectious morbidity in children with acute lymphoblastic leukemia (ALL).PROCEDURE: In a prospective study, 43 children receiving treatment for ALL were monitored for mucosal toxicity from diagnosis through the induction phase of treatment. Serial blood draws were taken to determine the levels of SP-D, interleukin-6 (IL-6), C-reactive protein, and white blood cells. Data on fever, antibiotics, and bacteremia were collected. Baseline levels of circulating SP-D were compared with healthy controls.RESULTS: Baseline values of circulating SP-D were similar to levels in healthy controls (median: 829 ng/ml vs. 657 ng/ml, respectively, P > 0.05). After initiation of chemotherapy, a significant reduction in SP-D levels was observed at all time points: 704 ng/ml at day 8, 413 ng/ml at day 15, 395 ng/ml at day 22, and 520 ng/ml at day 29 (all, P < 0.05). No significant associations between SP-D values, the occurrence of mucosal toxicity, or infectious morbidity were observed. However, loss of circulating SP-D from days 8 to 15 was associated with more systemic inflammation, and lower SP-D values at day 15 were associated with elevated intestinal mucositis scores (P < 0.05).CONCLUSIONS: The current study supports the hypothesis that the detrimental effect of chemotherapy on patients' immune functions includes decreased circulating levels of innate mucosal molecules such as SP-D, potentially aggravating mucosal and systemic inflammatory responses.",
author = "Mathias Rathe and Sorensen, {Grith L.} and Wehner, {Peder S.} and Uffe Holmskov and Sangild, {Per T.} and Kjeld Schmiegelow and Klaus M{\"u}ller and Steffen Husby",
note = "{\textcopyright} 2016 Wiley Periodicals, Inc.",
year = "2017",
doi = "10.1002/pbc.26253",
language = "English",
volume = "64",
journal = "Pediatric Blood & Cancer",
issn = "1545-5009",
publisher = "JohnWiley & Sons, Inc.",
number = "3",

}

RIS

TY - JOUR

T1 - Chemotherapeutic treatment reduces circulating levels of surfactant protein-D in children with acute lymphoblastic leukemia

AU - Rathe, Mathias

AU - Sorensen, Grith L.

AU - Wehner, Peder S.

AU - Holmskov, Uffe

AU - Sangild, Per T.

AU - Schmiegelow, Kjeld

AU - Müller, Klaus

AU - Husby, Steffen

N1 - © 2016 Wiley Periodicals, Inc.

PY - 2017

Y1 - 2017

N2 - BACKGROUND: Surfactant protein D (SP-D) is a host defense molecule of the innate immune system that enhances pathogen clearance and modulates inflammatory responses. We hypothesized that circulating SP-D levels are associated with chemotherapy-induced mucositis and infectious morbidity in children with acute lymphoblastic leukemia (ALL).PROCEDURE: In a prospective study, 43 children receiving treatment for ALL were monitored for mucosal toxicity from diagnosis through the induction phase of treatment. Serial blood draws were taken to determine the levels of SP-D, interleukin-6 (IL-6), C-reactive protein, and white blood cells. Data on fever, antibiotics, and bacteremia were collected. Baseline levels of circulating SP-D were compared with healthy controls.RESULTS: Baseline values of circulating SP-D were similar to levels in healthy controls (median: 829 ng/ml vs. 657 ng/ml, respectively, P > 0.05). After initiation of chemotherapy, a significant reduction in SP-D levels was observed at all time points: 704 ng/ml at day 8, 413 ng/ml at day 15, 395 ng/ml at day 22, and 520 ng/ml at day 29 (all, P < 0.05). No significant associations between SP-D values, the occurrence of mucosal toxicity, or infectious morbidity were observed. However, loss of circulating SP-D from days 8 to 15 was associated with more systemic inflammation, and lower SP-D values at day 15 were associated with elevated intestinal mucositis scores (P < 0.05).CONCLUSIONS: The current study supports the hypothesis that the detrimental effect of chemotherapy on patients' immune functions includes decreased circulating levels of innate mucosal molecules such as SP-D, potentially aggravating mucosal and systemic inflammatory responses.

AB - BACKGROUND: Surfactant protein D (SP-D) is a host defense molecule of the innate immune system that enhances pathogen clearance and modulates inflammatory responses. We hypothesized that circulating SP-D levels are associated with chemotherapy-induced mucositis and infectious morbidity in children with acute lymphoblastic leukemia (ALL).PROCEDURE: In a prospective study, 43 children receiving treatment for ALL were monitored for mucosal toxicity from diagnosis through the induction phase of treatment. Serial blood draws were taken to determine the levels of SP-D, interleukin-6 (IL-6), C-reactive protein, and white blood cells. Data on fever, antibiotics, and bacteremia were collected. Baseline levels of circulating SP-D were compared with healthy controls.RESULTS: Baseline values of circulating SP-D were similar to levels in healthy controls (median: 829 ng/ml vs. 657 ng/ml, respectively, P > 0.05). After initiation of chemotherapy, a significant reduction in SP-D levels was observed at all time points: 704 ng/ml at day 8, 413 ng/ml at day 15, 395 ng/ml at day 22, and 520 ng/ml at day 29 (all, P < 0.05). No significant associations between SP-D values, the occurrence of mucosal toxicity, or infectious morbidity were observed. However, loss of circulating SP-D from days 8 to 15 was associated with more systemic inflammation, and lower SP-D values at day 15 were associated with elevated intestinal mucositis scores (P < 0.05).CONCLUSIONS: The current study supports the hypothesis that the detrimental effect of chemotherapy on patients' immune functions includes decreased circulating levels of innate mucosal molecules such as SP-D, potentially aggravating mucosal and systemic inflammatory responses.

U2 - 10.1002/pbc.26253

DO - 10.1002/pbc.26253

M3 - Journal article

C2 - 27667327

VL - 64

JO - Pediatric Blood & Cancer

JF - Pediatric Blood & Cancer

SN - 1545-5009

IS - 3

M1 - e26253

ER -

ID: 172431047