# Are There General Features of How Immune Responses Are Regulated That Can Provide Clues to How Remitting/Relapsing Multiple Sclerosis May Be Treated?

**Authors:** Peter Alan Bretscher

PMC · DOI: 10.3390/ijms25052726 · International Journal of Molecular Sciences · 2024-02-27

## TL;DR

The paper explores how immune responses to complex antigens might be regulated, offering insights into treating remitting/relapsing multiple sclerosis.

## Contribution

Proposes a novel mechanism for immune regulation in remitting/relapsing multiple sclerosis involving complex antigens.

## Key findings

- Immune responses to complex antigens differ from those to simple antigens in regulation.
- A proposed mechanism explains the fluctuating inflammatory state in multiple sclerosis.
- The mechanism suggests a potential non-invasive treatment approach.

## Abstract

Most basic studies directed at how immune responses are regulated employ chemically “simple antigens”, usually purified proteins. The target antigens in many clinical situations, such as in autoimmunity, infectious diseases and cancer, are chemically “complex”, consisting of several distinct molecules, and they often are part of a replicating entity. We examine here the relationships between how immune responses to complex and simple antigens are regulated. This examination provides a context for considering how immune responses are regulated in those clinical situations involving complex antigens. I have proposed and discuss here a mechanism by which immune responses to the envisaged complex target antigen in remitting/relapsing multiple sclerosis go back and forth between inflammatory and non-inflammatory modes, potentially accounting for the course of this disease. This proposal makes predictions that can be tested by non-invasive means. It also leads to a suggestion for simple, non-invasive treatment.

## Linked entities

- **Diseases:** multiple sclerosis (MONDO:0005301)

## Full-text entities

- **Diseases:** Multiple Sclerosis (MESH:D009103), infectious diseases (MESH:D003141), inflammatory (MESH:D007249), cancer (MESH:D009369)

## Full text

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## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC10932258/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC10932258/full.md

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Source: https://tomesphere.com/paper/PMC10932258