# A comparative study on immune responses to demineralized and decellularized bone substitute following intraperitoneal implantation in mouse model

**Authors:** K. G. Aghila Rani, Ali Al Qabbani, Sausan AlKawas, Manju Nidagodu Jayakumar, S. A. H. Suzina, A. R. Samsudin, Ahmad Azlina, Gianpaolo Papaccio, Gianpaolo Papaccio, Gianpaolo Papaccio

PMC · DOI: 10.1371/journal.pone.0323666 · PLOS One · 2025-05-16

## TL;DR

This study compares immune responses to two types of bone substitutes in mice, finding that decellularized bone shows better immune tolerance.

## Contribution

The study provides new insights into the immunocompatibility of demineralized and decellularized bone substitutes in a mouse model.

## Key findings

- DCC substitutes showed reduced inflammation and immune response compared to DMB.
- DCC group exhibited normal organ morphology similar to sham-operated controls.
- DMB showed higher cytokine levels and T-cell counts compared to DCC.

## Abstract

The immunological sensitization of implanted bone grafts is crucial for long-term success. This study aimed to investigate the immune responses following implantation of lyophilized demineralized (DMB) and lyophilized decellularized (DCC) bovine cancellous bone substitutes, respectively, in mouse models of peritoneal implantation to evaluate the effectiveness of DMB and DCC processing methods. The DMB and DCC substitutes were prepared using published methods. BALB/c mice were divided into four groups (n = 4). A small abdominal incision was created to deliver the DMB or DCC materials into the peritoneal cavity. The first group received native unprocessed bone, while the second group was sham-operated (SO). The third and fourth groups received DMB and DCC substitutes, respectively. The immunogenicity effects of the implants were assessed through WBC count, spleen index, CD4 + /CD8 + counts, cytokine expression, and histology analysis of the spleen, liver and kidney. Native controls displayed systemic inflammation. The DMB group showed an increased trend in WBC count, cytokine profile and spleen index on day seven, followed by a considerable reduction in the DCC group compared to DMB on days 14 and 21. The native group showed significantly higher CD4+ /CD8+  T-cells and proinflammatory cytokines (IL-12, TNF-α, IFN-γ, MCP-1, IL-6). Additionally, the DMB group showed significantly higher mRNA levels for IL-1β, TNF-α, IL-6, and the anti-inflammatory cytokine IL-10. The DMB group further exhibited a significantly higher CD4 +  count, while the DCC group demonstrated higher CD8+  T-cells on day 1. Histological assessments of the liver and kidney revealed pyknotic nuclei, necrotic cells, and extravasated RBCs in the native group and, to a lesser extent, in the DMB group, while the DCC group showed normal morphology similar to Sham. Both DMB and DCC demonstrated favourable immunocompatibility properties, while DCC exhibited further immune tolerance in the mouse model.

## Linked entities

- **Proteins:** IL1B (interleukin 1 beta), TNF (tumor necrosis factor), IL6 (interleukin 6), IL10 (interleukin 10), IL12 (Interleukin 12 level), TNF (tumor necrosis factor), IFNG (interferon gamma), CCL2 (C-C motif chemokine ligand 2), IL6 (interleukin 6), CD4 (CD4 molecule), CD8A (CD8 subunit alpha)

## Full-text entities

- **Genes:** Cd247 (CD247 antigen) [NCBI Gene 12503] {aka 4930549J05Rik, A430104F18Rik, Cd3, Cd3-eta, Cd3-zeta, Cd3h}, Ifng (interferon gamma) [NCBI Gene 15978] {aka IFN-g, If2f, Ifg}, Dcc (DCC netrin 1 receptor) [NCBI Gene 13176] {aka C030036D22Rik, Igdcc1}, Il10 (interleukin 10) [NCBI Gene 16153] {aka CSIF, If2a, Il-10}, Apc (APC, WNT signaling pathway regulator) [NCBI Gene 11789] {aka CC1, Min, mAPC}, Cd4 (CD4 antigen) [NCBI Gene 12504] {aka L3T4, Ly-4}, Hmgb1 (high mobility group box 1) [NCBI Gene 15289] {aka HMG-1, Hmg1, SBP-1, p30}, Il6 (interleukin 6) [NCBI Gene 16193] {aka Il-6}, Mcpt1 (mast cell protease 1) [NCBI Gene 17224] {aka Mcp-1}, S100a1 (S100 calcium binding protein A1) [NCBI Gene 20193] {aka S100, S100a}, Tnf (tumor necrosis factor) [NCBI Gene 21926] {aka DIF, TNF-a, TNF-alpha, TNFSF2, TNFalpha, Tnfa}, Il1 (interleukin 1 complex) [NCBI Gene 111343] {aka Il-1}, DCC (DCC netrin 1 receptor) [NCBI Gene 1630] {aka CRC18, CRCR1, HGPPS2, IGDCC1, MRMV1, NTN1R1}, CD4 (CD4 molecule) [NCBI Gene 407098], Il1b (interleukin 1 beta) [NCBI Gene 16176] {aka IL-1beta, Il-1b}
- **Diseases:** necrotic (MESH:D009336), DEMINERALIZED (MESH:D017001), pain (MESH:D010146), systemic (MESH:D015619), kidney tissue damage (MESH:D007674), Inflammation (MESH:D007249), cervical dislocation (MESH:D002575), bone defect (MESH:D001847), immunological injury (MESH:D007154), hepatosplenomegaly (MESH:C535727), hemorrhage (MESH:D006470), splenomegaly (MESH:D013163), cytotoxic (MESH:D064420), hypertrophy (MESH:D006984)
- **Chemicals:** eosin (MESH:D004801), hydroxyapatite (MESH:D017886), DMB (MESH:C002037), PBS (MESH:D007854), xylazine (MESH:D014991), SYBR green (MESH:C098022), calcium phosphate (MESH:C020243), paraffin (MESH:D010232), hematoxylin (MESH:D006416), Bupresol (-), H&amp;E (MESH:D006371), betadine (MESH:D011206), formalin (MESH:D005557), water (MESH:D014867), Cy5.5 (MESH:C098793)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606], Bos taurus (bovine, species) [taxon 9913]
- **Cell lines:** c — Mus musculus (Mouse), Hepatocellular carcinoma of the mouse, Cancer cell line (CVCL_9103)

## Full text

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## Figures

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## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC12084032/full.md

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Source: https://tomesphere.com/paper/PMC12084032