Mucosal calprotectin is associated with severity of aGI-GVHD and poor outcomes after allogeneic stem cell transplantation

E Ekin Ece Gurer Kluge (1Clinic and Polyclinic for Internal Medicine III, University Hospital Regensburg, Regensburg, Germany) E Elisabeth Meedt J Julia Feicht (1Clinic and Polyclinic for Internal Medicine III, University Hospital Regensburg, Regensburg, Germany) K Kedi Cao (1Clinic and Polyclinic for Internal Medicine III, University Hospital Regensburg, Regensburg, Germany) A Andreas Hiergeist A Andreas Mamilos D Daniela Hirsch M Matthias Hoepting (1Clinic and Polyclinic for Internal Medicine III, University Hospital Regensburg, Regensburg, Germany) A Anna-Sophia Kattner (1Clinic and Polyclinic for Internal Medicine III, University Hospital Regensburg, Regensburg, Germany) C Carina Matos (1Clinic and Polyclinic for Internal Medicine III, University Hospital Regensburg, Regensburg, Germany) S Sigrid Bülow (5Institute of Clinical Microbiology and Hygiene, University Hospital Regensburg, Regensburg, Germany) E Erik Thiele Orberg P Philipp Beckhove A Arne Kandulski M Matthias Evert K Kai Hildner M Marina Kreutz M Matthias Edinger D Daniel Wolff W Wolfgang Herr H Hendrik Poeck A André Gessner D Daniela Weber B Birte Kehr (3Leibniz Institute for Immunotherapy, Regensburg, Germany) E Ernst Holler S Sakhila Ghimire

Abstract

Abstract Calprotectin, a calcium- and zinc-binding protein that comprises the subunits S100A8 and S100A9, has been extensively studied as a biomarker of gastrointestinal (GI) inflammation through fecal and serum analyses. However, its role in intestinal tissue remains poorly understood because of the limited availability of biopsy specimens. In this study, we analyzed S100A8 and S100A9 messenger RNA (mRNA) expression in 579 intestinal biopsy specimens from allogeneic stem cell transplantation recipients and observed a strong association with acute GI graft-versus-host disease (aGI-GVHD; P< .001). Neutrophil infiltration correlated with the severity of aGI-GVHD (P< .001), and calprotectin expression was strongly linked to Toll-like receptor 4 (TLR4; P< .001) and TLR2 (P< .001) expression. Both TLR4 and aGI-GVHD were associated with elevated calprotectin mRNA levels (P< .001). When patients received broad-spectrum antibiotics at disease onset, calprotectin expression was suppressed (S100A8, P = .001; S100A9, P = .01). GI site–specific differences in calprotectin expression were identified: during severe aGI-GVHD, levels increased up to 30-fold in the small intestine and up to fivefold in the large intestine with respect to mild or no aGI-GVHD, whereas under homeostasis, the large intestine exhibited higher baseline calprotectin (P = .001). The high clinical relevance of this finding is evident from the observation that calprotectin expression was prognostic for transplant-related mortality. Our study suggests that (1) calprotectin is a potential biopsy biomarker in aGI-GvHD and (2) calprotectin expression and neutrophil infiltration possibly indicate translocation of microbiota, which (3) may be modulated by antibiotics.

Article Details

Journal Blood
Volume / Issue Vol. 147, Issue 8
Published February 19, 2026
Pages 886-896
ISSN 0006-4971
Publisher Elsevier BV

Journal Info

Blood

Elsevier BV

ISSN: 0006-4971 Health Sciences

Authors (26)

E

Ekin Ece Gurer Kluge

1Clinic and Polyclinic for Internal Medicine III, University Hospital Regensburg, Regensburg, Germany

E

Elisabeth Meedt

J

Julia Feicht

1Clinic and Polyclinic for Internal Medicine III, University Hospital Regensburg, Regensburg, Germany

K

Kedi Cao

1Clinic and Polyclinic for Internal Medicine III, University Hospital Regensburg, Regensburg, Germany

A

Andreas Hiergeist

A

Andreas Mamilos

D

Daniela Hirsch

M

Matthias Hoepting

1Clinic and Polyclinic for Internal Medicine III, University Hospital Regensburg, Regensburg, Germany

A

Anna-Sophia Kattner

1Clinic and Polyclinic for Internal Medicine III, University Hospital Regensburg, Regensburg, Germany

C

Carina Matos

1Clinic and Polyclinic for Internal Medicine III, University Hospital Regensburg, Regensburg, Germany

S

Sigrid Bülow

5Institute of Clinical Microbiology and Hygiene, University Hospital Regensburg, Regensburg, Germany

E

Erik Thiele Orberg

P

Philipp Beckhove

A

Arne Kandulski

M

Matthias Evert

K

Kai Hildner

M

Marina Kreutz

M

Matthias Edinger

D

Daniel Wolff

W

Wolfgang Herr

H

Hendrik Poeck

A

André Gessner

D

Daniela Weber

B

Birte Kehr

3Leibniz Institute for Immunotherapy, Regensburg, Germany

E

Ernst Holler

S

Sakhila Ghimire