» Articles » PMID: 28513269

Immune Surveillance in Melanoma: From Immune Attack to Melanoma Escape and Even Counterattack

Overview
Specialties Oncology
Pharmacology
Date 2017 May 18
PMID 28513269
Citations 24
Authors
Affiliations
Soon will be listed here.
Abstract

Pharmacologic inhibition of the cytotoxic T lymphocyte antigen 4 (CTLA4) and the programmed death receptor-1 (PD1) has resulted in unprecedented durable responses in metastatic melanoma. However, resistance to immunotherapy remains a major challenge. Effective immune surveillance against melanoma requires 4 essential steps: activation of the T lymphocytes, homing of the activated T lymphocytes to the melanoma microenvironment, identification and episode of melanoma cells by activated T lymphocytes, and the sensitivity of melanoma cells to apoptosis. At each of these steps, there are multiple factors that may interfere with the immune surveillance machinery, thus allowing melanoma cells to escape immune attack and develop resistance to immunotherapy. We provide a comprehensive review of the complex immune surveillance mechanisms at play in melanoma, and a detailed discussion of how these mechanisms may allow for the development of intrinsic or acquired resistance to immunotherapeutic modalities, and potential avenues for overcoming this resistance.

Citing Articles

Inflammasome activation in melanoma progression: the latest update concerning pathological role and therapeutic value.

Pluetrattanabha N, Direksunthorn T, Ahmad I, Jyothi S, Shit D, Singh A Arch Dermatol Res. 2025; 317(1):258.

PMID: 39820618 DOI: 10.1007/s00403-025-03802-1.


Canine Adipose-Derived Mesenchymal Stromal Cells Reduce Cell Viability and Migration of Metastatic Canine Oral Melanoma Cell Lines In Vitro.

Teng F, de Faria Lainetti P, Simao Franzoni M, Fernando Leis Filho A, Massoco Salles Gomes C, Laufer-Amorim R Vet Sci. 2024; 11(12).

PMID: 39728976 PMC: 11680336. DOI: 10.3390/vetsci11120636.


Exploring the Surface: Sampling of Potential Skin Cancer Biomarkers Kynurenine and Tryptophan, Studied on 3D Melanocyte and Melanoma Models.

Hasterok S, Jankovskaja S, Miletic Dahlstrom R, Prgomet Z, Ohlsson L, Bjorklund S Biomolecules. 2024; 14(7).

PMID: 39062529 PMC: 11274760. DOI: 10.3390/biom14070815.


Impact of Genomic Mutation on Melanoma Immune Microenvironment and IFN-1 Pathway-Driven Therapeutic Responses.

Mentucci F, Romero Nunez E, Ercole A, Silvetti V, Dal Col J, Lamberti M Cancers (Basel). 2024; 16(14).

PMID: 39061208 PMC: 11274745. DOI: 10.3390/cancers16142568.


Immune escape and metastasis mechanisms in melanoma: breaking down the dichotomy.

Shirley C, Chhabra G, Amiri D, Chang H, Ahmad N Front Immunol. 2024; 15:1336023.

PMID: 38426087 PMC: 10902921. DOI: 10.3389/fimmu.2024.1336023.


References
1.
Vucic D, Franklin M, Wallweber H, Das K, Eckelman B, Shin H . Engineering ML-IAP to produce an extraordinarily potent caspase 9 inhibitor: implications for Smac-dependent anti-apoptotic activity of ML-IAP. Biochem J. 2004; 385(Pt 1):11-20. PMC: 1134668. DOI: 10.1042/BJ20041108. View

2.
Griffith T, Brunner T, Fletcher S, Green D, Ferguson T . Fas ligand-induced apoptosis as a mechanism of immune privilege. Science. 1995; 270(5239):1189-92. DOI: 10.1126/science.270.5239.1189. View

3.
Contardi E, Palmisano G, Tazzari P, Martelli A, Fala F, Fabbi M . CTLA-4 is constitutively expressed on tumor cells and can trigger apoptosis upon ligand interaction. Int J Cancer. 2005; 117(4):538-50. DOI: 10.1002/ijc.21155. View

4.
Franco A, Zhang X, Van Berkel E, Sanders J, Zhang X, Thomas W . The role of NF-kappa B in TNF-related apoptosis-inducing ligand (TRAIL)-induced apoptosis of melanoma cells. J Immunol. 2001; 166(9):5337-45. DOI: 10.4049/jimmunol.166.9.5337. View

5.
Thomas W, Hersey P . TNF-related apoptosis-inducing ligand (TRAIL) induces apoptosis in Fas ligand-resistant melanoma cells and mediates CD4 T cell killing of target cells. J Immunol. 1998; 161(5):2195-200. View