# Changes in immune cell signatures during early infection reflect decoupling of capillary perfusion and glycocalyx dimensions

## TL;DR

The study shows that changes in immune cells during early infection are linked to damage in the glycocalyx, a layer on blood vessel walls, and not just to capillary density.

## Contribution

The novel finding is that glycocalyx damage is associated with specific immune cell signatures, distinct from capillary perfusion changes.

## Key findings

- Glycocalyx damage correlates with unique immune cell subsets like monocytes and T-cells.
- Two immune endotypes were identified: one with suppressed immunity and higher severity, the other with enhanced immunity and lower severity.
- Capillary density changes were not linked to immune endotypes or glycocalyx dimensions.

## Abstract

Microvascular injury is central to the pathophysiology of sepsis, but its interaction with the immune system in early infection is unclear. This study aimed to phenotype peripheral blood mononuclear cells (PBMC) from emergency department (ED) patients with suspected bacterial infection and correlate the results with microvascular changes.

This prospective observational study included 49 adult ED patients with suspected infection and 17 healthy controls. Capillary density and glycocalyx dimensions were measured by sublingual microscopy, while peripheral blood immune cell subsets were analyzed by deep flow cytometry.

Network visualization of 72 diIerentially regulated parameters revealed specific changes in diIerent immune cell subsets. Innate immune changes included a functional diversion of monocytes towards pathogen defense and tissue repair, whereas adaptive immune changes included the development of CD4+ T cells with Th2-profile and cytotoxic CD8+ T cells. Unsupervised clustering revealed two distinct immune endotypes: E1 with a suppressed immune response and higher disease severity, and E2 with an enhanced immune response and lower disease severity. Patients showed significant reductions in capillary density and glycocalyx dimensions, which were neither correlated in magnitude nor associated with endotypes. There was a strong association between damaged glycocalyx and several monocyte and T-cell subsets. This association was not observed for capillary density.

We demonstrate that glycocalyx damage is associated with a unique immunological signature, distinct from functional capillary density. These findings provide a strong basis for future studies of immune dysregulation and microvascular dysfunction in infection.