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Susceptibility to Cryptococcus neoformans Infection with Bruton's Tyrosine Kinase Inhibition.

Publication ,  Journal Article
Messina, JA; Giamberardino, CD; Tenor, JL; Toffaletti, DL; Schell, WA; Asfaw, YG; Palmucci, JR; Lionakis, MS; Perfect, JR
Published in: Infect Immun
August 16, 2023

Patients receiving the Bruton's tyrosine kinase (BTK) inhibitor ibrutinib have an increased likelihood of fungal infections. The objectives of this study were to determine if Cryptococcus neoformans infection severity was isolate dependent with BTK inhibition and whether blocking BTK impacted infection severity in a mouse model. We compared four clinical isolates from patients on ibrutinib to virulent (H99) and avirulent (A1-35-8) reference strains. BTK knockout (KO) and wild-type (WT) C57 mice and WT CD1 mice were infected by intranasal (i.n.), oropharyngeal aspiration (OPA), and intravenous (i.v.) routes. Infection severity was assessed by survival and fungal burden (CFU per gram of tissue). Ibrutinib (25 mg/kg) or vehicle was administered daily through intraperitoneal injections. In the BTK KO model, no isolate-dependent effect on fungal burden was observed, and infection severity was not significantly different from that of the WT with i.n., OPA, and i.v. routes. Ibrutinib treatment did not impact infection severity. However, when the four clinical isolates were compared to H99, two of these isolates were less virulent, with significantly longer survival and reduced rates of brain infection. In conclusion, C. neoformans infection severity in the BTK KO model does not appear to be isolate dependent. BTK KO and ibrutinib treatment did not result in significantly different infection severities. However, based on repeated clinical observations of increased susceptibility to fungal infections with BTK inhibitor therapy, further work is needed to optimize a mouse model with BTK inhibition to better understand the role that this pathway plays in susceptibility to C. neoformans infection.

Duke Scholars

Published In

Infect Immun

DOI

EISSN

1098-5522

Publication Date

August 16, 2023

Volume

91

Issue

8

Start / End Page

e0004223

Location

United States

Related Subject Headings

  • Protein Kinase Inhibitors
  • Microbiology
  • Mice
  • Cryptococcosis
  • Brain
  • Animals
  • Agammaglobulinaemia Tyrosine Kinase
  • 3207 Medical microbiology
  • 3204 Immunology
  • 3107 Microbiology
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Messina, J. A., Giamberardino, C. D., Tenor, J. L., Toffaletti, D. L., Schell, W. A., Asfaw, Y. G., … Perfect, J. R. (2023). Susceptibility to Cryptococcus neoformans Infection with Bruton's Tyrosine Kinase Inhibition. Infect Immun, 91(8), e0004223. https://doi.org/10.1128/iai.00042-23
Messina, Julia A., Charles D. Giamberardino, Jennifer L. Tenor, Dena L. Toffaletti, Wiley A. Schell, Yohannes G. Asfaw, Julia R. Palmucci, Michail S. Lionakis, and John R. Perfect. “Susceptibility to Cryptococcus neoformans Infection with Bruton's Tyrosine Kinase Inhibition.Infect Immun 91, no. 8 (August 16, 2023): e0004223. https://doi.org/10.1128/iai.00042-23.
Messina JA, Giamberardino CD, Tenor JL, Toffaletti DL, Schell WA, Asfaw YG, et al. Susceptibility to Cryptococcus neoformans Infection with Bruton's Tyrosine Kinase Inhibition. Infect Immun. 2023 Aug 16;91(8):e0004223.
Messina, Julia A., et al. “Susceptibility to Cryptococcus neoformans Infection with Bruton's Tyrosine Kinase Inhibition.Infect Immun, vol. 91, no. 8, Aug. 2023, p. e0004223. Pubmed, doi:10.1128/iai.00042-23.
Messina JA, Giamberardino CD, Tenor JL, Toffaletti DL, Schell WA, Asfaw YG, Palmucci JR, Lionakis MS, Perfect JR. Susceptibility to Cryptococcus neoformans Infection with Bruton's Tyrosine Kinase Inhibition. Infect Immun. 2023 Aug 16;91(8):e0004223.

Published In

Infect Immun

DOI

EISSN

1098-5522

Publication Date

August 16, 2023

Volume

91

Issue

8

Start / End Page

e0004223

Location

United States

Related Subject Headings

  • Protein Kinase Inhibitors
  • Microbiology
  • Mice
  • Cryptococcosis
  • Brain
  • Animals
  • Agammaglobulinaemia Tyrosine Kinase
  • 3207 Medical microbiology
  • 3204 Immunology
  • 3107 Microbiology