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  • Open Access

Use of CD137 up-regulation to identify T cell receptors specifically reactive with mutated tumor associated antigens from tumor infiltrating lymphocytes

  • 1,
  • 2,
  • 3,
  • 3,
  • 4,
  • 1,
  • 1 and
  • 5
Journal for ImmunoTherapy of Cancer20153 (Suppl 2) :P40

https://doi.org/10.1186/2051-1426-3-S2-P40

  • Published:

Keywords

  • Metastatic Melanoma
  • Exome Sequencing
  • Adoptive Transfer
  • Tumor Infiltrate Lymphocyte
  • Tumor Associate Antigen

Background

The adoptive transfer of tumor infiltrating lymphocytes (TIL) can mediate the regression of metastatic melanoma. In addition, the adoptive transfer of lymphocytes genetically modified to express tumor reactive T cell receptors (TCRs) can mediate tumor regression. Many T cells from TIL recognize mutated antigens expressed only on the autologous patient's tumors. Therefore, we attempted to isolate TCRs reactive with unique mutated antigens so that we might eventually be able to treat patients with autologous T cells genetically modified to express those TCRs.

Methods

Mutations in tumors were identified using whole exome sequencing and/or RNA sequencing. Tandem minigene (TMG) constructs containing 12-24 minigenes were synthesized, each encoding the mutated amino acid flanked by 12 amino acids on both sides. RNAs encoding the TMGs were in vitro transcribed and electroporated into autologous dendritic cells (DCs). Recognition of TMGs by TIL was evaluated on the basis of IFN-γ secretion and CD137 expression after overnight coculture with the electroporated DCs. Subsequently, mutation reactive T cells were enriched from TIL by sorting for CD137+ T cells after overnight coculture with the electroporated DCs and were expanded in vitro with anti-CD3 and IL-2. Dominant TCR α and β chain sequences were identified in the enriched mutation reactive populations, and retroviruses encoding those TCRs were used to transduce human PBL to determine if they mediated recognition of the mutated antigen.

Results

Thus far, using these techniques we have isolated mutation reactive TCRs from 6 different patients with metastatic melanoma as described in the attached table. We are currently extending these techniques to identify mutation reactive TCRs for patients with other cancers including those of the gastrointestinal tract, breast, and ovaries. We are also developing clinical reagents to treat patients with TCRs that recognize unique mutations on autologous tumor cells.
Table 1

Mutation reactive TCRs identified by CD137 upregulation.

Patient

Mutated antigen

# of independent TCRs

3466

COL18A1

1

3466

ERBB2

1

3903

KIAA1279

3

3903

KIAA1967

1

3903

PHKA1

1

3784

FLNA

1

3784

KIF16B

3

3678

FBOX21

1

3678

RECQL5

2

3716

Not yet identified at individual gene level

1

4000

Not yet identified at individual gene level

Up to 4

Authors’ Affiliations

(1)
NIH/NCI/Surgery Branch, Bethesda, MD, USA
(2)
NCI/NIH, Bethesda, MD, USA
(3)
Surgery Branch/National Cancer Institute / National Institutes of Health, Bethesda, MD, USA
(4)
NCI/NIH, Rutgers Robert Wood Johnson Medical School, New Brunswick, NJ, USA
(5)
NIH/NCI, Bethesda, MD, USA

Copyright

© Parkhurst et al. 2015

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

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