Nature Communications (Dec 2024)

Compassionate access to virus-specific T cells for adoptive immunotherapy over 15 years

  • Michelle A. Neller,
  • George R. Ambalathingal,
  • Nada Hamad,
  • Joe Sasadeusz,
  • Rebecca Pearson,
  • Chien-Li Holmes-Liew,
  • Deepak Singhal,
  • Matthew Tunbridge,
  • Wei Yang Ng,
  • Kirsty Sharplin,
  • Andrew Moore,
  • David Deambrosis,
  • Trisha Soosay-Raj,
  • Peter McNaughton,
  • Morag Whyte,
  • Chris Fraser,
  • Andrew Grigg,
  • David Kliman,
  • Ashish Bajel,
  • Katherine Cummins,
  • Mark Dowling,
  • Zhi Han Yeoh,
  • Simon J. Harrison,
  • Amit Khot,
  • Sarah Tan,
  • Izanne Roos,
  • Ray Mun Koo,
  • Sara Dohrmann,
  • David Ritchie,
  • Brynn Wainstein,
  • Karen McCleary,
  • Adam Nelson,
  • Bradley Gardiner,
  • Shafqat Inam,
  • Xavier Badoux,
  • Kris Ma,
  • Claudia Toro,
  • Diane Hanna,
  • David Hughes,
  • Rachel Conyers,
  • Theresa Cole,
  • Shiqi Stacie Wang,
  • Lynette Chee,
  • Jacqueline Fleming,
  • Ashley Irish,
  • Duncan Purtill,
  • Julian Cooney,
  • Peter Shaw,
  • Siok-Keen Tey,
  • Stewart Hunt,
  • Elango Subramonia Pillai,
  • George John,
  • Michelle Ng,
  • Shanti Ramachandran,
  • Peter Hopkins,
  • Daniel Chambers,
  • Scott Campbell,
  • Ross Francis,
  • Nicole Isbel,
  • Paula Marlton,
  • Hilary Reddiex,
  • Katherine K. Matthews,
  • Meggie Voogt,
  • Archana Panikkar,
  • Leone Beagley,
  • Sweera Rehan,
  • Shannon Best,
  • Jyothy Raju,
  • Laetitia Le Texier,
  • Pauline Crooks,
  • Matthew Solomon,
  • Lea Lekieffre,
  • Sriganesh Srihari,
  • Corey Smith,
  • Rajiv Khanna

DOI
https://doi.org/10.1038/s41467-024-54595-2
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 12

Abstract

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Abstract Adoptive T-cell immunotherapy holds great promise for the treatment of viral complications in immunocompromised patients resistant to standard anti-viral strategies. We present a retrospective analysis of 78 patients from 19 hospitals across Australia and New Zealand, treated over the last 15 years with “off-the-shelf” allogeneic T cells directed to a combination of Epstein–Barr virus (EBV), cytomegalovirus (CMV), BK polyomavirus (BKV), John Cunningham virus (JCV) and/or adenovirus (AdV) under the Australian Therapeutic Goods Administration’s Special Access Scheme. Most patients had severe post-transplant viral complications, including drug-resistant end-organ CMV disease, BKV-associated haemorrhagic cystitis and EBV-driven post-transplant lymphoproliferative disorder. Adoptive immunotherapy is well tolerated with few adverse effects. Importantly, 46/71 (65%) patients show definitive clinical improvement including reduction in viral load, clinical symptoms and complete resolution of end-organ disease. In addition, seven high-risk patients remain disease free. Based on this long-term encouraging clinical experience, we propose that a dedicated nationally funded centre for anti-viral cellular therapies should be considered to provide T cell therapies for critically ill patients for compassionate use.