Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2013 Dec;48(4):242-9.
doi: 10.5045/br.2013.48.4.242. Epub 2013 Dec 24.

Next generation sequencing: new tools in immunology and hematology

Affiliations
Review

Next generation sequencing: new tools in immunology and hematology

Antonio Mori et al. Blood Res. 2013 Dec.

Abstract

One of the hallmarks of the adaptive immune system is the specificity of B and T cell receptors. Thanks to somatic recombination, a large repertoire of receptors can be generated within an individual that guarantee the recognition of a vast number of antigens. Monoclonal antibodies have limited applicability, given the high degree of diversity among these receptors, in BCR and TCR monitoring. Furthermore, with regard to cancer, better characterization of complex genomes and the ability to monitor tumor-specific cryptic mutations or translocations are needed to develop better tailored therapies. Novel technologies, by enhancing the ability of BCR and TCR monitoring, can help in the search for minimal residual disease during hematological malignancy diagnosis and follow-up, and can aid in improving bone marrow transplantation techniques. Recently, a novel technology known as next generation sequencing has been developed; this allows the recognition of unique sequences and provides depth of coverage, heterogeneity, and accuracy of sequencing. This provides a powerful tool that, along with microarray analysis for gene expression, may become integral in resolving the remaining key problems in hematology. This review describes the state of the art of this novel technology, its application in the immunological and hematological fields, and the possible benefits it will provide for the hematology and immunology community.

Keywords: B cell receptor; Immune monitoring; Next generation sequence; T cell receptor.

PubMed Disclaimer

Conflict of interest statement

No potential conflicts of interest relevant to this article were reported.

Figures

Fig. 1
Fig. 1
Next generation sequencing second-generation platforms: comparison and workflow.

References

    1. Tonegawa S, Steinberg C, Dube S, Bernardini A. Evidence for somatic generation of antibody diversity. Proc Natl Acad Sci U S A. 1974;71:4027–4031. - PMC - PubMed
    1. Tonegawa S. Somatic generation of antibody diversity. Nature. 1983;302:575–581. - PubMed
    1. Kim S, Davis M, Sinn E, Patten P, Hood L. Antibody diversity: somatic hypermutation of rearranged VH genes. Cell. 1981;27:573–581. - PubMed
    1. Thomas L. On immunosurveillance in human cancer. Yale J Biol Med. 1982;55:329–333. - PMC - PubMed
    1. Burnet FM. Immunological aspects of malignant disease. Lancet. 1967;1:1171–1174. - PubMed