# Diagnostic value and challenges in the immune regulation of pentraxin 3 in infectious diseases

**Authors:** Teng-Hao Shao, Tie-Min Li, Jin-Wen Zhang, Xiao-Wei Lv, Xin-Tong Li, Na Cui, Ping Sheng

PMC · DOI: 10.3389/fmicb.2026.1777246 · Frontiers in Microbiology · 2026-02-20

## TL;DR

This review explores how pentraxin 3 (PTX3) could help diagnose infectious diseases more precisely, despite challenges in its immune regulation.

## Contribution

The paper systematically summarizes PTX3's diagnostic potential and immunomodulatory mechanisms in infectious diseases.

## Key findings

- PTX3 is rapidly produced by immune cells and shows promise as a biomarker for infectious diseases.
- PTX3 aids host defense through complement activation and inflammation modulation.
- Clinical use of PTX3 is limited by its broad inflammatory response and complex regulatory mechanisms.

## Abstract

Infectious diseases pose a severe threat to human health, and their early and precise diagnosis and intervention remain a major challenge in clinical practice. This review systematically examines the diagnostic value and immunomodulatory role of PTX3 across a spectrum of infectious diseases, including those affecting the respiratory, cardiovascular, digestive, urinary, and nervous systems, as well as orthopedic and skin infections. The aim is to provide novel perspectives for overcoming the bottleneck in precise diagnosis and treatment of infectious diseases. Currently, diagnosis and assessment primarily rely on clinical manifestations, conventional inflammatory markers such as C-reactive protein (CRP) and procalcitonin, and pathogen detection. However, these methods often have limitations in sensitivity, specificity, and early warning capability, underscoring the need for novel, high-value biomarkers to enhance diagnostic and therapeutic precision. Long pentraxin 3 (PTX3), a key acute-phase reactant protein and soluble pattern recognition receptor (PRR), has recently garnered considerable attention for its role in infectious diseases. PTX3 is rapidly synthesized by innate immune and endothelial cells in response to stimulation by pathogens or inflammatory mediators. Functionally, PTX3 contributes to host defense through opsonophagocytosis, complement activation, and modulation of inflammatory responses. Quantification of circulating PTX3 levels demonstrates potential as an adjunctive biomarker for the diagnosis of infectious diseases and holds considerable value in early risk stratification, precise disease assessment, and personalized therapeutic strategies. Nevertheless, the clinical application of PTX3 faces two major challenges in immune regulation. Its broad-spectrum responsiveness to inflammation limits its specificity in pathogen differentiation, and the mechanisms underlying its immunomodulatory activity remain complex. This review systematically summarizes recent advances in the diagnostic significance and immunoregulatory mechanisms of PTX3, providing new insights into overcoming current challenges in the precision diagnosis and treatment of infectious diseases.

## Linked entities

- **Proteins:** PTX3 (pentraxin 3), CRP (C-reactive protein)
- **Diseases:** respiratory infections (MONDO:0024355)

## Full-text entities

- **Genes:** C4B (complement C4B (Chido/Rodgers blood group)) [NCBI Gene 721] {aka C4B1, C4B12, C4B3, C4B5, C4BD, C4F}, C1QA (complement C1q A chain) [NCBI Gene 712] {aka C1QD1}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, Ccr6 (C-C motif chemokine receptor 6) [NCBI Gene 12458] {aka CC-CKR-6, CCR-6, Cmkbr6, KY411}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, PLG (plasminogen) [NCBI Gene 5340] {aka HAE4}, Ccl20 (C-C motif chemokine ligand 20) [NCBI Gene 20297] {aka CKb4, LARC, MIP-3A, MIP-3[a], MIP3A, ST38}, CCL20 (C-C motif chemokine ligand 20) [NCBI Gene 6364] {aka CKb4, Exodus, LARC, MIP-3-alpha, MIP-3a, MIP3A}, NEU1 (neuraminidase 1) [NCBI Gene 4758] {aka NANH, NEU, SIAL1}, PTX3 (pentraxin 3) [NCBI Gene 5806] {aka TNFAIP5, TSG-14}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, CFH (complement factor H) [NCBI Gene 3075] {aka AHUS1, AMBP1, ARMD4, ARMS1, CFHL3, FH}, Tfrc (transferrin receptor) [NCBI Gene 22042] {aka 2610028K12Rik, CD71, E430033M20Rik, Mtvr1, TFR, TFR1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, PTX4 (pentraxin 4) [NCBI Gene 390667] {aka C16orf38}, CSF2 (colony stimulating factor 2) [NCBI Gene 1437] {aka CSF, GMCSF}, Nlrp3 (NLR family, pyrin domain containing 3) [NCBI Gene 216799] {aka AGTAVPRL, AII/AVP, Cias1, FCAS, FCU, MWS}, SELP (selectin P) [NCBI Gene 6403] {aka CD62, CD62P, GMP140, GRMP, LECAM3, PADGEM}, IL17A (interleukin 17A) [NCBI Gene 3605] {aka CTLA-8, CTLA8, IL-17, IL-17A, IL17, ILA17}, APCS (amyloid P component, serum) [NCBI Gene 325] {aka HEL-S-92n, PTX2, SAP}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, TFRC (transferrin receptor) [NCBI Gene 7037] {aka CD71, IMD46, T9, TFR, TFR1, TR}, CCR6 (C-C motif chemokine receptor 6) [NCBI Gene 1235] {aka BN-1, C-C CKR-6, CC-CKR-6, CCR-6, CD196, CKR-L3}, Ptx3 (pentraxin related gene) [NCBI Gene 19288] {aka TSG-14}
- **Diseases:** meningitis (MESH:D008580), acute pancreatitis (MESH:D010195), abdominal pain (MESH:D015746), gallbladder perforation (MESH:D005705), diseases (MESH:D004194), injury (MESH:D014947), pulmonary infection (MESH:D012141), liver diseases (MESH:D008107), inflammation (MESH:D007249), mitochondrial dysfunction (MESH:D028361), hemorrhagic fever (MESH:D006480), fracture (MESH:D050723), myelopathy (MESH:D013118), acute pyelonephritis (MESH:D011704), Lyme neuroborreliosis (MESH:D020852), renal syndrome (MESH:D006030), Mucor species infections (MESH:C000656945), PJI (MESH:D057068), organ dysfunction (MESH:D009102), neurological diseases (MESH:D020271), digestive infections (MESH:D004828), infectious myocarditis (MESH:D009205), bacterial pneumonia (MESH:D018410), S. pneumoniae infection (MESH:D011014), COPD (MESH:D029424), cardiomyopathy (MESH:D009202), coronavirus disease 2019 (MESH:D000086382), alcoholic hepatitis (MESH:D006519), dilated cardiomyopathy (MESH:D002311), and skin infections (MESH:D007239), fungal pneumonia (MESH:D008172), cardiovascular injury (MESH:D002318), -acquired pneumonia (MESH:D000077299), digestive system disorders (MESH:D004066), RUTI (MESH:D014552), leprosy (MESH:D007918), endotoxemia (MESH:D019446), erythema nodosum leprosum (MESH:D004893), AA (MESH:D001064), bacterial meningitis (MESH:D016920), Pseudomonas aeruginosa infection (MESH:D011552), Streptococcus pneumoniae infection (MESH:D011008), viral meningitis (MESH:D008587), CNS infections (MESH:D002494), viral encephalitis (MESH:D018792), septic shock (MESH:D012772), fungal disease (MESH:D009181), Sepsis (MESH:D018805), severe acute pancreatitis (MESH:D045169), acute bacterial infections (MESH:D011472), Infectious diseases (MESH:D003141), invasive (MESH:D009361), CAP (MESH:D003147), cutaneous leishmaniasis (MESH:D016773), IA (MESH:D055744), renal dysfunction (MESH:D007674), orthopedic infections (MESH:D009140), bacterial infection (MESH:D001424), systemic (MESH:D015619), liver injury (MESH:D017093)
- **Chemicals:** sialic acid (MESH:D019158), PTXs (-), disulfide (MESH:D004220), creatinine (MESH:D003404), LPS (MESH:D008070), urea nitrogen (MESH:C530477)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Human T-cell leukemia virus type I (no rank) [taxon 11908], H3N2 subtype (serotype) [taxon 119210], Aspergillus fumigatus (species) [taxon 746128], Escherichia coli (E. coli, species) [taxon 562], Klebsiella (genus) [taxon 570], H1N1 subtype (serotype) [taxon 114727], Mycobacterium tuberculosis (species) [taxon 1773], Homo sapiens (human, species) [taxon 9606], Orthomyxoviridae (family) [taxon 11308]
- **Mutations:** rs3816527, rs2853550, (AUC) of 0

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## References

50 references — full list in the complete paper: https://tomesphere.com/paper/PMC12962959/full.md

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Source: https://tomesphere.com/paper/PMC12962959