# Surgical Primary Tumor Resection Reduces Accumulation of CD11b+ Myeloid Cells in the Lungs Augmenting the Efficacy of an Intranasal Cancer Vaccination against Secondary Lung Metastasis

**Authors:** Michael Donkor, Jamie Y. Choe, Danielle Marie Reid, Hope K. Fiadjoe, Byron Quinn, Amalendu Ranjan, Mark Pulse, Pankaj Chaudhary, Riyaz Basha, Harlan P. Jones

PMC · DOI: 10.3390/ph17010051 · Pharmaceuticals · 2023-12-28

## TL;DR

Surgery to remove a primary tumor, combined with a nasal vaccine, can reduce lung metastasis by altering immune cell accumulation.

## Contribution

The study introduces a nasal nano-vaccine that, when combined with surgery, reduces lung metastasis by modulating immune cell dynamics.

## Key findings

- Primary tumor resection reduces CD11b+ myeloid cell accumulation in the lungs.
- The nasal vaccine increases infiltration of T cells in the lungs of surgery mice.
- The vaccine significantly reduces lung metastasis in mice after surgery.

## Abstract

A hallmark of effective cancer treatment is the prevention of tumor reoccurrence and metastasis to distal organs, which are responsible for most cancer deaths. However, primary tumor resection is expected to be curative as most solid tumors have been shown both experimentally and clinically to accelerate metastasis to distal organs including the lungs. In this study, we evaluated the efficacy of our engineered nasal nano-vaccine (CpG-NP-Tag) in reducing accelerated lung metastasis resulting from primary tumor resection. Cytosine–phosphate–guanine oligonucleotide [CpG ODN]-conjugated nanoparticle [NP] encapsulating tumor antigen [Tag] (CpG-NP-Tag) was manufactured and tested in vivo using a syngeneic mouse mammary tumor model following intranasal delivery. We found that our nasal nano-vaccine (CpG-NP-Tag), compared to control NPs administered after primary mammary tumor resection, significantly reduced lung metastasis in female BALB/c mice subjected to surgery (surgery mice). An evaluation of vaccine efficacy in both surgery and non-surgery mice revealed that primary tumor resection reduces CD11b+ monocyte-derived suppressor-like cell accumulation in the lungs, allowing increased infiltration of vaccine-elicited T cells (IFN-γ CD8+ T cells) in the lungs of surgery mice compared to non-surgery mice. These findings suggest that the combination of the target delivery of a nasal vaccine in conjunction with the standard surgery of primary tumors is a plausible adjunctive treatment against the establishment of lung metastasis.

## Linked entities

- **Proteins:** ITGAM (integrin subunit alpha M), IFNG (interferon gamma), CD8A (CD8 subunit alpha)
- **Diseases:** cancer (MONDO:0004992)

## Full-text entities

- **Genes:** Ly6c1 (lymphocyte antigen 6 family member C1) [NCBI Gene 17067] {aka Ly-6C, Ly-6C1, Ly6c}, Cd28 (CD28 antigen) [NCBI Gene 12487], MMP9 (matrix metallopeptidase 9) [NCBI Gene 4318] {aka CLG4B, GELB, MANDP2, MMP-9}, Gzmb (granzyme B) [NCBI Gene 14939] {aka CCP-1/C11, CCP1, Ctla-1, Ctla1, GZB}, Ly6g (lymphocyte antigen 6 family member G) [NCBI Gene 546644] {aka Gr-1, Gr1, Ly-6G}, ITGAM (integrin subunit alpha M) [NCBI Gene 3684] {aka CD11B, CR3A, HNA-4, MAC-1, MAC1A, MO1A}, Cd4 (CD4 antigen) [NCBI Gene 12504] {aka L3T4, Ly-4}, Ifng (interferon gamma) [NCBI Gene 15978] {aka IFN-g, If2f, Ifg}, Cd69 (CD69 antigen) [NCBI Gene 12515] {aka 5830438K24Rik, AIM, VEA}, Ptprc (protein tyrosine phosphatase receptor type C) [NCBI Gene 19264] {aka B220, CD45R, Cd45, L-CA, Ly-5, Lyt-4}, Itgae (integrin alpha E, epithelial-associated) [NCBI Gene 16407] {aka A530055J10, CD103, aM290, alpha-E1, alpha-M290}, Tlr9 (toll-like receptor 9) [NCBI Gene 81897], D9Mgc45e (DNA segment, Chr 9, MRC UK Mouse Genome Centre 45 expressed) [NCBI Gene 28134] {aka CD3}, Itgam (integrin alpha M) [NCBI Gene 16409] {aka CD11b/CD18, CR3, CR3A, Cd11b, F730045J24Rik, Ly-40}
- **Diseases:** melanoma (MESH:D008545), lung lesion (MESH:D008171), carcinogenic (MESH:D011230), injury to people or property (MESH:C000719191), lung tumor (MESH:D008175), inflammation (MESH:D007249), Mammary Tumor (MESH:D015674), -Derived (MESH:C536408), Primary Tumors (MESH:D001932), Lung Metastasis (MESH:D009362), metastatic lung nodules (MESH:D003074), mammary adenocarcinoma (MESH:D000230), pain (MESH:D010146), Tag (MESH:D009369), metastatic (MESH:D000092182), Breast tumors (MESH:D001943)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Mutations:** S18009F
- **Cell lines:** 4T1 — Mus musculus (Mouse), Malignant neoplasms of the mouse mammary gland, Cancer cell line (CVCL_0125), BALB/c — Mus musculus (Mouse), Spontaneously immortalized cell line (CVCL_0184), H1.2F3 — Mus musculus (Mouse), Hybridoma (CVCL_B0HJ), B-XMG1.2 — Mus musculus (Mouse), Hybridoma (CVCL_2H37), BALB/ — Mus musculus (Mouse), Transformed cell line (CVCL_4350), S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10821475/full.md

## References

39 references — full list in the complete paper: https://tomesphere.com/paper/PMC10821475/full.md

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Source: https://tomesphere.com/paper/PMC10821475