» Articles » PMID: 30307119

Clinical Proteomics for Post-Hematopoeitic Stem Cell Transplantation Outcomes

Overview
Specialty Biochemistry
Date 2018 Oct 12
PMID 30307119
Citations 5
Authors
Affiliations
Soon will be listed here.
Abstract

Allogeneic hematopoietic stem cell transplantation (HSCT) is the most effective form of tumor immunotherapy available to date. However, while HSCT can induce beneficial graft-versus-leukemia (GVL) effect, the adverse effect of graft-versus-host disease (GVHD), which is closely linked to GVL, is the major source of morbidity and mortality following HSCT. Until recently, available diagnostic and staging tools frequently fail to identify those at higher risk of disease progression or death. Furthermore, there are shortcomings in the prediction of the need for therapeutic interventions or the response rates to different forms of therapy. The past decade has been characterized by an explosive evolution of proteomics technologies, largely due to important advances in high-throughput MS instruments and bioinformatics. Building on these opportunities, blood biomarkers have been identified and validated both as promising diagnostic tools, prognostic tools that risk-stratify patients before future occurrence of GVHD and as predictive tools for responsiveness to GVHD therapy and non-relapse mortality. These biomarkers might facilitate timely and selective therapeutic intervention. This review summarizes current information on clinical proteomics for GVHD as well as other complications following HSCT. Finally, it proposes future directions for the translation of clinical proteomics to discovery of new potential therapeutic targets to the development of drugs.

Citing Articles

Insights gained from single-cell analysis of chimeric antigen receptor T-cell immunotherapy in cancer.

Tang L, Huang Z, Mei H, Hu Y Mil Med Res. 2023; 10(1):52.

PMID: 37941075 PMC: 10631149. DOI: 10.1186/s40779-023-00486-4.


Relevant proteins for the monitoring of engraftment phases after allogeneic hematopoietic stem cell transplantation.

Souza M, Coutinho-Camillo C, Paula F, de Paula F, Bologna S, Lourenco S Clinics (Sao Paulo). 2022; 77:100134.

PMID: 36403426 PMC: 9678684. DOI: 10.1016/j.clinsp.2022.100134.


Longitudinal proteomics study of serum changes after allogeneic HSCT reveals potential markers of metabolic complications related to aGvHD.

Wong S, Kato S, Rodenburg F, Tojo A, Hayashi N Sci Rep. 2022; 12(1):14002.

PMID: 35977993 PMC: 9385631. DOI: 10.1038/s41598-022-18221-9.


A biomarker panel for risk of early respiratory failure following hematopoietic cell transplantation.

Rowan C, Smith L, Sharron M, Loftis L, Kudchadkar S, Duncan C Blood Adv. 2022; 6(6):1866-1878.

PMID: 35139145 PMC: 8941462. DOI: 10.1182/bloodadvances.2021005770.


An overview of multiplexed analyses of CAR T-cell therapies: insights and potential.

DePriest B, Vieira N, Bidgoli A, Paczesny S Expert Rev Proteomics. 2021; 18(9):767-780.

PMID: 34628995 PMC: 8626704. DOI: 10.1080/14789450.2021.1992276.

References
1.
Schaub S, Rush D, Wilkins J, Gibson I, Weiler T, Sangster K . Proteomic-based detection of urine proteins associated with acute renal allograft rejection. J Am Soc Nephrol. 2003; 15(1):219-27. DOI: 10.1097/01.asn.0000101031.52826.be. View

2.
Pepe M, Etzioni R, Feng Z, Potter J, Thompson M, Thornquist M . Phases of biomarker development for early detection of cancer. J Natl Cancer Inst. 2001; 93(14):1054-61. DOI: 10.1093/jnci/93.14.1054. View

3.
Kaiser T, Kamal H, Rank A, Kolb H, Holler E, Ganser A . Proteomics applied to the clinical follow-up of patients after allogeneic hematopoietic stem cell transplantation. Blood. 2004; 104(2):340-9. DOI: 10.1182/blood-2004-02-0518. View

4.
Boja E, Hiltke T, Rivers R, Kinsinger C, Rahbar A, Mesri M . Evolution of clinical proteomics and its role in medicine. J Proteome Res. 2010; 10(1):66-84. DOI: 10.1021/pr100532g. View

5.
Levine J, Logan B, Wu J, Alousi A, Bolanos-Meade J, Ferrara J . Acute graft-versus-host disease biomarkers measured during therapy can predict treatment outcomes: a Blood and Marrow Transplant Clinical Trials Network study. Blood. 2012; 119(16):3854-60. PMC: 3335389. DOI: 10.1182/blood-2012-01-403063. View