G-Rex® for Virus-Specific T-Cell Therapy

The simplest way to assemble quality virus-specific T-cell therapies.

From single-virus products to multivirus-specific T-cell banks, G-Rex® supports flexible, scalable manufacturing for autologous and allogeneic VST therapies.

The Value of Simplicity

In virus-specific T-cell therapy, simplicity is the ultimate sophistication.

Virus-specific T-cell manufacturing must accommodate different donors, viral targets, antigen-presentation strategies and product models.

G-Rex® provides one simple expansion platform that can support this diversity—from patient- or donor-specific products to scalable banks of multivirus-specific T cells.

Simplified expansion

G-Rex® eliminates the convoluted, manipulation-heavy workflows that have historically made VST manufacturing inaccessible

Flexible & Versatile

G-Rex® supports VST manufacturing across single-virus or multi-virus workflows, across diverse viral targets, and donor types.

Clinically Translatable

G-Rex® has a well-documented history supporting the translation of virus specific T cell therapies from R&D to GMP.

The Gold Standard

The gold standard for virus-specific T-cell therapy.

For more than 15 years, the Center for Cell and Gene Therapy at Baylor College of Medicine, Houston Methodist Hospital and Texas Children’s Hospital has used G-Rex® to help advance virus-specific T-cell manufacturing—from rapidly generated donor-specific products to multivirus-specific T cells and third-party VST banks.

That adoption has extended to leading academic and clinical institutions, including Children’s National Hospital, Great Ormond Street Hospital, University College London, Hôpital Maisonneuve-Rosemont, Institut Cochin and Banc de Sang i Teixits. Across these institutions, G-Rex® has supported VSTs targeting CMV, EBV, adenovirus, BK virus, HHV-6 and other clinically important viruses.

G-Rex® has continued to support VST manufacturing as the field progressed from institution-specific clinical programs to third-party cell banks and a commercially approved allogeneic virus-specific T-cell therapy. Across academia and industry, G-Rex® has become the gold standard for virus-specific T-cell manufacturing.

G-Rex

Baylor College of Medicine

Houston Methodist Hospital

Texas Children's Hospital

Children’s National Hospital

Great Ormond Street Hospital

University College London

Columbia University

Memorial Sloan Kettering

Banc de Sang i Teixits

Scottish National Blood Transfusion Service

Hôpital Maisonneuve-Rosemont

NIH National Institutes of Health

Explore the Evidence →

A Typical Process

Virus-specific T-cell therapy manufacturing made simple.

VST manufacturing begins with cells collected from a patient, stem-cell donor or healthy third-party donor. Antigen-specific T cells are stimulated or selected against one or more viral targets, expanded in G-Rex®, harvested and prepared for administration or cryopreserved for future use.

Patient

Recommended Products

Build your virus-specific T-cell manufacturing platform in G-Rex®.

The G-Rex® product family supports virus-specific T-cell manufacturing from small-scale process development through clinical production. Select the G-Rex® format that aligns with your starting cell number, required dose and manufacturing model.

Explore G-Rex® Products →

Next Steps

Whatever phase your virus-specific T-cell program is at, a G-Rex® Optimization Specialist can help.

Whether you are developing a new VST process, transitioning an existing workflow into G-Rex®, optimizing clinical manufacturing or scaling a third-party VST bank, our team can help you identify the right G-Rex® products and process strategy for your program.

Frequently Asked Questions

Frequently asked questions about G-Rex® for virus-specific T-cell therapy.

Which viruses can virus-specific T cells (VSTs) manufactured in G-Rex® target?

Published G-Rex® workflows include VSTs targeting CMV, EBV, adenovirus, BK virus, HHV-6, HIV and other clinically important viruses.

Can G-Rex® support multivirus-specific T-cell products?

Yes. G-Rex® has been used to manufacture VST products targeting multiple viruses simultaneously, including three-, four- and five-virus-specific products.

Can G-Rex® support both autologous and allogeneic VST manufacturing?

Yes. Published workflows include patient-derived, stem-cell-donor-derived, healthy-donor-derived and third-party VST products.

What starting materials can be used for VST manufacturing in G-Rex®?

Published workflows have used peripheral blood mononuclear cells, leukapheresis material and umbilical cord blood.

Where does G-Rex® fit within a typical VST manufacturing process?

G-Rex® can support both the initial stimulation or pulsing of cells with viral peptide pools and their subsequent expansion. Initial stimulation is typically performed at a low working volume of approximately 1 mL/cm², followed by expansion at a larger working volume of approximately 10 mL/cm².

Can G-Rex® support third-party VST banks?

Yes. G-Rex® has supported the manufacture of cryopreserved third-party VST banks designed to provide partially HLA-matched products for multiple recipients.

Can VSTs be genetically engineered in a G-Rex®-based workflow?

Yes. Published workflows have incorporated genetic modification, including CAR and lentiviral engineering. Genetic modification can be performed directly in G-Rex® before continued expansion.

Have a different question? Connect with a G-Rex® Optimization Specialist.

Evidence & References

Peer-reviewed evidence from academia and industry.

Explore the published evidence supporting the use of G-Rex across virus-specific T-cell research, development, and clinical manufacturing.

  1. Vera JF, et al. Accelerated production of antigen-specific T cells for preclinical and clinical applications using gas-permeable rapid expansion cultureware (G-Rex). Journal of Immunotherapy. 2010;33(3):305–315. doi:10.1097/CJI.0b013e3181c0c3cb.
  2. Bollard CM, et al. Manufacture of GMP-grade cytotoxic T lymphocytes specific for LMP1 and LMP2 for patients with EBV-associated lymphoma. Cytotherapy. 2011;13(5):518–522. doi:10.3109/14653249.2011.561983.
  3. Lapteva N, Vera JF. Optimization manufacture of virus- and tumor-specific T cells. Stem Cells International. 2011;2011:434392. doi:10.4061/2011/434392.
  4. Sili U, et al. Production of good manufacturing practice-grade cytotoxic T lymphocytes specific for Epstein–Barr virus, cytomegalovirus and adenovirus to prevent or treat viral infections post-allogeneic hematopoietic stem cell transplant. Cytotherapy. 2012;14(1):7–11. doi:10.3109/14653249.2011.636963.
  5. Gerdemann U, et al. Rapidly generated multivirus-specific cytotoxic T lymphocytes for the prophylaxis and treatment of viral infections. Molecular Therapy. 2012;20:1622–1632. doi:10.1038/mt.2012.130.
  6. Gerdemann U, et al. Safety and clinical efficacy of rapidly generated trivirus-directed T cells as treatment for adenovirus, EBV, and CMV infections after allogeneic hematopoietic stem cell transplant. Molecular Therapy. 2013;21(11):2113–2121. doi:10.1038/mt.2013.151.
  7. Papadopoulou A, et al. Adoptive transfer of rapidly-generated multivirus-specific T cells to treat Adv, EBV, CMV, BK and HHV6 infections of HSCT recipients. Journal for ImmunoTherapy of Cancer. 2013;1(Suppl 1):O2. doi:10.1186/2051-1426-1-S1-O2.
  8. Sun J, et al. Early transduction produces highly functional chimeric antigen receptor-modified virus-specific T-cells with central memory markers: A Production Assistant for Cell Therapy (PACT) translational application. Journal for ImmunoTherapy of Cancer. 2015;3:5. doi:10.1186/s40425-015-0049-1.
  9. Spielmann G, et al. A single exercise bout enhances the manufacture of viral-specific T-cells from healthy donors: Implications for allogeneic adoptive transfer immunotherapy. Scientific Reports. 2016;6:25852. doi:10.1038/srep25852.
  10. Horlock C, et al. Manufacture of GMP-compliant functional adenovirus-specific T-cell therapy for treatment of post-transplant infectious complications. Cytotherapy. 2016. doi:10.1016/j.jcyt.2016.06.009.
  11. Lamarche C, et al. Clinical-scale rapid autologous BK virus-specific T cell line generation from kidney transplant recipients with active viremia for adoptive immunotherapy. Transplantation. 2017. doi:10.1097/TP.0000000000001698.
  12. Dave H, et al. Toward a rapid production of multivirus-specific T cells targeting BKV, adenovirus, CMV, and EBV from umbilical cord blood. Molecular Therapy: Methods & Clinical Development. 2017;5:13–21. doi:10.1016/j.omtm.2017.02.001.
  13. Kuranda K, et al. In vitro expansion of anti-viral T cells from cord blood by accelerated co-cultured dendritic cells. Molecular Therapy: Methods & Clinical Development. 2019;13:112–120. doi:10.1016/j.omtm.2018.12.010.
  14. Tzannou I, et al. “Mini” bank of only 8 donors supplies CMV-directed T cells to diverse recipients. Blood Advances. 2019;3(17):2571–2580. doi:10.1182/bloodadvances.2019000371.
  15. Grau-Vorster M, et al. Characterization of a cytomegalovirus-specific T lymphocyte product obtained through a rapid and scalable production process for use in adoptive immunotherapy. Frontiers in Immunology. 2020;11:271. doi:10.3389/fimmu.2020.00271.
  16. Li H, et al. Preclinical development and clinical-scale manufacturing of HIV Gag-specific, lentivirus-modified CD4 T cells for HIV functional cure. Molecular Therapy: Methods & Clinical Development. 2020;17:1048–1060. doi:10.1016/j.omtm.2020.04.024.
  17. Lazarski CA, et al. Identification of new cytokine combinations for antigen-specific T-cell therapy products via a high-throughput multi-parameter assay. Cytotherapy. 2020. doi:10.1016/j.jcyt.2020.08.006.
  18. Soni MK, et al. The prospect of universal coronavirus immunity: Characterization of reciprocal and non-reciprocal T cell responses against SARS-CoV-2 and common human coronaviruses. Frontiers in Immunology. 2023;14:1212203. doi:10.3389/fimmu.2023.1212203.
  19. Cooper RS, et al. EBV T-cell immunotherapy generated by peptide selection has enhanced effector functionality compared to LCL stimulation. Frontiers in Immunology. 2024;15:1412211. doi:10.3389/fimmu.2024.1412211.
  20. Palianina D, et al. Stem cell memory EBV-specific T cells control EBV tumor growth and persist in vivo. Science Advances. 2024;10(34):eado2048. doi:10.1126/sciadv.ado2048.
  21. ElAbd H, et al. T and B cell responses against Epstein–Barr virus in primary sclerosing cholangitis. Nature Medicine. 2025. doi:10.1038/s41591-025-03692-w.
  22. Wang, X., & Rivière, I. (2015). Manufacture of tumor- and virus-specific T lymphocytes for adoptive cell therapies. Cancer Gene Therapy, 22, 85–94. doi:10.3389/fimmu.2024.1412211