# High procalcitonin in Gram-negative urosepsis: indicator of immune modulation rather than poor outcome

**Authors:** Sebastian Petzoldt, Christina Buschhaus, Matthias Hecker, Arne Hauptmann, Florian Wagenlehner, Matthias Wolff, Martin Reichert, Veronika Grau, Andreas Hecker, Markus Weigand, Anca-Laura Amati

PMC · DOI: 10.1007/s00345-026-06199-2 · World Journal of Urology · 2026-02-27

## TL;DR

High procalcitonin levels in Gram-negative urosepsis may indicate a protective immune response rather than a poor prognosis.

## Contribution

The study reveals a novel immunomodulatory role of procalcitonin in Gram-negative urosepsis by inhibiting IL-1β secretion.

## Key findings

- Procalcitonin significantly inhibits IL-1β secretion from primary mononuclear leukocytes in a concentration-dependent manner.
- Patients with Gram-negative urosepsis and procalcitonin levels between 2.5–75 µg/L had lower SOFA scores and lactate levels, indicating less severe disease.
- High procalcitonin levels in Gram-negative urosepsis are associated with a protective host response rather than worse outcomes.

## Abstract

Procalcitonin (PCT) is an acute-phase protein and widely used marker for diagnosing bacterial infection and sepsis, but its physiological role remains incompletely defined. Interleukin-1β (IL-1β) is a critical mediator of the immune response to infection, whose excessive release can drive remote organ injury and dysfunction. Its secretion is therefore tightly controlled. Because other acute-phase proteins have been shown to regulate IL-1β secretion, we investigated whether PCT exerts a similar immunomodulatory effect and whether this influences sepsis severity, particularly in Gram-negative urosepsis.

Primary human mononuclear leukocytes were stimulated to induce IL-1β release in the presence or absence of increasing PCT concentrations. In parallel, peak PCT levels, infection source, and causative pathogen were analyzed retrospectively in uroseptic patients in comparison to other septic sources, and related to Sepsis-related Organ Failure Assessment (SOFA) scores and serum lactate concentrations.

PCT significantly inhibited IL-1β secretion from primary mononuclear leukocytes across the 2.5–75 µg/L concentration range. Clinically, the highest PCT peaks occurred in patients with Gram-negative urosepsis. Among these, those with peak PCT values within 2.5–75 µg/L had significantly lower SOFA scores and lactate levels—established indicators of sepsis severity and prognosis—compared with patients outside this range.

Within a defined concentration range, PCT down-regulates IL-1β secretion and is associated with reduced markers of disease severity in Gram-negative urosepsis, compared to other sepsis entities. These findings suggest that pronounced PCT elevations in this setting may represent a protective host response rather than a worse prognosis, pointing to a novel immunomodulatory role of PCT in urosepsis that warrants further investigation.

DRKS00037950, retrospectively registered on 22 September 2025.

The online version contains supplementary material available at 10.1007/s00345-026-06199-2.

## Linked entities

- **Proteins:** IL1B (interleukin 1 beta)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, SERPINA1 (serpin family A member 1) [NCBI Gene 5265] {aka A1A, A1AT, AAT, PI, PI1, PRO2275}, VN1R17P (vomeronasal 1 receptor 17 pseudogene) [NCBI Gene 441931] {aka GPCR}, CXCR6 (C-X-C motif chemokine receptor 6) [NCBI Gene 10663] {aka BONZO, CD186, CDw186, STRL33, TYMSTR}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, CCL2 (C-C motif chemokine ligand 2) [NCBI Gene 6347] {aka GDCF-2, HC11, HSMCR30, MCAF, MCP-1, MCP1}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, NOS2 (nitric oxide synthase 2) [NCBI Gene 4843] {aka HEP-NOS, INOS, NOS, NOS2A}, P2RX7 (purinergic receptor P2X 7) [NCBI Gene 5027] {aka P2X7}, CALCA (calcitonin related polypeptide alpha) [NCBI Gene 796] {aka CALC1, CGRP, CGRP-I, CGRP-alpha, CGRP1, CT}
- **Diseases:** Pseudomonas (MESH:D011552), bronchopulmonary infections (MESH:D001997), cytotoxicity (MESH:D064420), infection (MESH:D007239), abdominal and pulmonary sepsis (MESH:D000007), bacterial (MESH:D001424), Sepsis (MESH:D018805), autoimmune, or chronic infectious diseases (MESH:D003141), septic (MESH:D001170), septic shock (MESH:D012772), Gram (MESH:D016908), trauma (MESH:D014947), respiratory infection (MESH:D012141), inflammation (MESH:D007249), multiorgan failure (MESH:D051437), Sepsis-related Organ Failure (MESH:D009102)
- **Chemicals:** 2'(3')-O-(4-benzoylbenzoyl)adenosine-5'-triphosphate (-), LPS (MESH:D008070), ATP (MESH:D000255), BzATP (MESH:C033901), lactate (MESH:D019344)
- **Species:** Homo sapiens (human, species) [taxon 9606], Pseudomonas (RNA similarity group I, genus) [taxon 286], Escherichia coli (E. coli, species) [taxon 562], Proteus (genus) [taxon 210425]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12948892/full.md

## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC12948892/full.md

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Source: https://tomesphere.com/paper/PMC12948892