# MZB1 at the ER-immunity interface: from antibody folding to disease vulnerability in autoimmunity, inflammation, and cancer

**Authors:** Yu Zhang, Wei Yang, Xiaofang Yang, Yuqing Pan, Rong Guo, Dong Chen, Shicong Tang, Xi Zhang

PMC · DOI: 10.7150/jca.125922 · 2026-02-11

## TL;DR

MZB1 is a protein involved in antibody folding and is linked to autoimmunity, inflammation, and cancer, making it a potential biomarker and therapeutic target.

## Contribution

This paper reviews the role of MZB1 in immune function and disease, highlighting its potential as a biomarker and therapeutic target.

## Key findings

- MZB1 facilitates IgM and IgA folding and is linked to autoantibody production in autoimmune diseases.
- MZB1 is overexpressed in certain cancers but silenced in others, affecting prognosis and tumor progression.
- MZB1's tissue-specific expression suggests potential for diagnostic and therapeutic applications.

## Abstract

MZB1 (marginal zone B and B1 cell-specific protein 1) is an endoplasmic reticulum-resident molecular chaperone that is predominantly expressed in marginal zone B cells, B1 cells, plasma cells, and pDCs. Functioning as a co-chaperone of GRP94 and BiP, MZB1 selectively facilitates the proper folding and secretion of immunoglobulin M (IgM) and J-chain-containing immunoglobulin A (IgA) dimers, and maintains the homeostasis of highly secretory cells by upregulating the expression of partner proteins such as BiP/GRP94. This review highlights the emerging role of MZB1 across various pathological conditions. In autoimmune diseases such as systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA), MZB1 contributes to aberrant autoantibody and cytokine secretion. MZB1 also modulates inflammatory responses in conditions such as colitis and periodontitis by regulating the B cell-skewed inflammatory microenvironment. In oncology, MZB1 is overexpressed in breast cancer (BC), lymphoma, and multiple myeloma (MM), where it is associated with enhanced tumor cell proliferation and poor prognosis. Conversely, in hepatocellular carcinoma (HCC) and gastric cancer (GC), MZB1 is transcriptionally silenced due to promoter hypermethylation. In summary, the tissue-specific expression pattern of MZB1 endows it with potential as both a diagnostic biomarker and therapeutic target, holding significant implications for the exploration of future cancer prognosis and treatment strategies.

## Linked entities

- **Genes:** MZB1 (marginal zone B and B1 cell specific protein) [NCBI Gene 51237]
- **Proteins:** HSP90B1 (heat shock protein 90 beta family member 1), GDF10 (growth differentiation factor 10), CD40LG (CD40 ligand), CD79A (CD79a molecule), JCHAIN (joining chain of multimeric IgA and IgM)
- **Diseases:** systemic lupus erythematosus (MONDO:0007915), rheumatoid arthritis (MONDO:0008383), colitis (MONDO:0005292), periodontitis (MONDO:0005076), breast cancer (MONDO:0004989), lymphoma (MONDO:0003659), multiple myeloma (MONDO:0009693), hepatocellular carcinoma (MONDO:0007256), gastric cancer (MONDO:0001056)

## Full-text entities

- **Genes:** HSPA5 (heat shock protein family A (Hsp70) member 5) [NCBI Gene 3309] {aka BIP, GRP78, HEL-S-89n}, CD79A (CD79a molecule) [NCBI Gene 973] {aka IGA, IGAlpha, MB-1, MB1}, MZB1 (marginal zone B and B1 cell specific protein) [NCBI Gene 51237] {aka MEDA-7, PACAP, pERp1}, HSP90B1 (heat shock protein 90 beta family member 1) [NCBI Gene 7184] {aka ECGP, GP96, GRP94, HEL-S-125m, HEL35, TRA1}
- **Diseases:** MM (MESH:D009101), HCC (MESH:D006528), GC (MESH:D013274), RA (MESH:D001172), SLE (MESH:D008180), autoimmune diseases (MESH:D001327), cancer (MESH:D009369), periodontitis (MESH:D010518), BC (MESH:D001943), lymphoma (MESH:D008223), colitis (MESH:D003092), inflammation (MESH:D007249)

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13003553/full.md

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Source: https://tomesphere.com/paper/PMC13003553