Lloyd J. Old

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Dr. Lloyd J. Old, M.D., c. 1995

Lloyd John Old (September 23, 1933 – November 28, 2011) was one of the founders and standard-bearers of the field of cancer immunology.[1] When Old began his career in 1958, tumor immunology was in its infancy. Today, cancer immunotherapies are emerging as a significant advance in cancer therapy.[2]

Old’s contributions to research established many of the principles and priorities of modern tumor immunology. In earlier work, he and his colleagues introduced Bacillus Calmette-Guérin (BCG) to tumor immunotherapy; discovered the first link between the major histocompatibility complex (MHC) and disease (leukemia); found the unexpected association between Epstein-Barr virus (EBV) and nasopharyngeal carcinoma; discovered Tumor necrosis factors (TNF); defined the concept of cell-surface differentiation antigens with the discovery of TL, Lyt (CD8), and a range of other mouse antigenic systems; discovered p53, independently with two other groups; and identified the tumor immunogenicity of heat shock proteins. Old is the author or co-author of more than 800 research publications. He was also a teacher helping young scientist as they began their career.

He held the William E. Snee Chair of Cancer Immunology at Memorial Sloan-Kettering Cancer Center (MSKCC), where he was director of the Ludwig Institute for Cancer Research (LICR) New York Branch. He was also a trustee of the LICR Charitable Trust, and a trustee of the Virginia & D.K. Ludwig Fund for Cancer Research.6. From 1971 to 2011, he served as the founding scientific and medical director of the Cancer Research Institute (CRI), where from 2001 to 2011 he also served as director of the CRI/LICR Cancer Vaccine Collaborative (CVC), an international network dedicated to testing and optimizing therapeutic cancer vaccines. Old’s previous appointments included Chairman of the LICR Board of Directors (2006–2009), LICR Scientific Director (1988 to 2005), Member of the Emeritus LICR Scientific Committee (1971–86), LICR Chief Executive Officer (1995–2004), and Associate Director of Research at MSKCC (1973–83).

Old served as a member of scientific advisory boards and committees including the Public Health Research Institute of the City of New York, the National Cancer Institute, and the American Association for Cancer Research. Old was also a member of the American Association for Cancer Research, New York Academy of Sciences, Reticuloendothelial Society, Society of Experimental Biology and Medicine, American Association for the Advancement of Science, American Association of Immunologists, National Academy of Sciences, the Academy of Cancer Immunology, and the American Academy of Arts and Sciences. He had also received honorary doctor of medicine degrees from Karolinska Institute, the University of Lausanne, and the University College London. He graduated from the University of California, Berkeley with a B.A. in biology and earned a medical degree from the University of California, San Francisco.

Old died November 28, 2011, in his New York City home, after several years battling advanced prostate cancer.[1]

Major Discoveries[edit]

  • Introduced Bacille Calmette-Guérin (BCG), the tuberculosis vaccine, into experimental cancer research as a way to stimulate non-specific resistance to tumor growth. BCG was FDA-approved in 1991 and is now widely used as a first line treatment for superficial bladder cancer (1959).[3]
  • Discovered the first linkage between the major histocompatibility complex (MHC) and disease—mouse leukemia—opening the way for the recognition of the importance of the MHC in the immune response (1964).[4]
  • Identified the first cell surface antigens distinguishing cells of different lineages, introducing the concept of cell surface antigens that could differentiate different cell types. First coined TL (for “thymus-leukemia” antigen in mice) then later as the Ly series (originally named Ly-A and Ly-B and later called Ly-1, Ly-2, and Ly-3), this discovery led directly to the wide use of cell surface markers to distinguish and classify normal and malignant cells and the development of CD classification (for “clusters of differentiation”). Most notably, Dr. Old discovered the LY-B antigen, later renamed CD8 in humans. CD8 cells, often referred to as “killer” T cells, are one of the major cells of the adaptive immune response, and are capable of directly killing dangerous or foreign cells (1964-1968).[5][6][7][8][9]
  • Discovery of the association between Epstein-Barr Virus (EBV) and nasopharyngeal cancer (1966).[10]
  • Discovery of tumor necrosis factor (TNF), a key immune signaling molecule (cytokine) that, in addition to its promise for the treatment of cancer and other diseases, has provided a powerful research tool in biomedicine (nearly 88,000 articles in PubMed as of May 25, 2011) (1975).[11][12]
  • Identification (independently, along with two other groups) of the p53 protein, the gene for which is mutated in approximately 50 percent of cancers (1979).[13]
  • Conducting of the most comprehensive dissection of the cell surface of human cancers using monoclonal antibodies, with the identification of an array of cell surface antigens as targets for antibody-based therapies of human cancer. Of the monoclonal antibodies developed in Dr. Old’s laboratory, thirteen have been licensed and seven are in clinical trials. These include:
    • the anti-EGFr antibody Hu806, which Abbott Laboratories acquired exclusive world-wide rights to develop in a major licensing deal in 2008. Hu806 targets the overexpressed form of the epidermal growth factor receptor (EGFr) present in 50 percent of all cancers of epithelial origin.[14]
    • cG250 (girentuximab, Rencarex®/Redectane®), which targets the CA-IX molecule/G250 antigen, expressed on over 90 percent of clear cells renal cell carcinomas (RCC, kidney cancer), and is in phase III clinical trials as a diagnostic tool and as a therapeutic modality (also iodine-131-G250).
    • hu3S193, which targets the LeY antigen, an oligosaccharide epitope expressed on glycolipids and glycoproteins by a wide range of epithelial cancers, is in phase II clinical trials being conducted by LICR spin-off company Recepta Biopharma.
    • huA33, which targets the A33 antigen present on colorectal cancer cells. The antibody has been licensed to LICR spin-off company Life Sciences Pharmaceuticals, and the mAb’s therapeutic potential is being tested as a stand-alone antibody, as a radioimmunotherapy agent, and in combination with chemotherapy.[15]
  • Establishment of the autologous typing system as the methodology leading to the identification of the first specific human tumor antigens recognized by antibodies and T cells, created 150 separate cancer cell lines, and laid the groundwork for the development of SEREX by Pfreundschuh in 1995.[16]
  • Discovery and naming of several members of the CT (cancer/testis) family of human tumor antigens, including New York-ESO-1 (NY-ESO-1). NY-ESO-1 is one of the most immunogenic human tumor antigens discovered to date and is expressed in approximately 35 percent of melanomas, 30 percent of breast cancers, 30 percent of liver cancers, 25 percent of lung cancers, less than five percent of colon cancers.
  • Establishment in 2001 of the Cancer Vaccine Collaborative (CVC), the world's first network of clinical trial sites closely linked with immunological monitoring laboratories with the goal to develop effective therapeutic cancer vaccines by first understanding the fundamental immunological implications of vaccination and applying that knowledge toward the rational design of optimal vaccine formulations. A joint program of the Cancer Research Institute and the Ludwig Institute for Cancer Research, the CVC conducts parallel, early phase, single variable clinical trials of various cancer vaccine formulations and combinations composed of cancer-specific antigen, immunological adjuvant, vaccine delivery platforms, and modulators of immune suppression.
  • Founder of "The Academy of Cancer Immunology [which] was established in 1998 to advance understanding of the role of immunity in cancer and to recognize outstanding achievements in the field of cancer immunology. The Academy currently has 53 members from 11 countries and holds annual elections for Academy membership." [20]

Leadership[edit]

As Director of the international Ludwig Institute for Cancer Research for 17 years, Scientific Director of the Cancer Research Institute for 40 years, and his previous appointment as Associate Director of Research at Memorial Sloan-Kettering Cancer Center for 10 years, Dr. Old guided the scientific vision of several institutions and the training and development of generations of young scientists in many fields.

Lloyd J. Old, M.D., c. 1974

Memorial Sloan-Kettering Cancer Center (MSKCC)

  • Memorial Hospital for Cancer and Allied Diseases
    • 1973-1976: Vice President and Associate Director
    • 1976-1986: Vice President and Associate Director for Scientific Development
  • Memorial Sloan-Kettering Cancer Center
    • 1973-1983: Associate Director of Research
  • Ludwig Institute for Cancer Research, New York Branch at MSKCC
    • Director, 1990–2011

Ludwig Institute for Cancer Research (LICR)

  • 1988-2005: Director
  • 1989–present: Member, Board of Directors
  • 1995-2004: Chief Executive Officer
  • 2006-2008: Chairman, Board of Directors

Virginia and Daniel K. Ludwig Trust

Lloyd J. Old, M.D., with Cancer Research Institute founder Helen Coley Nauts, Cancer Research Institute (CRI)
  • 1968-1971: Scientific Advisor
  • 1971-2011: Scientific Director

CRI/LICR Cancer Vaccine Collaborative (CVC)

  • 2001-2011: Director

Awards[edit]

References[edit]

  1. ^ a b Vitello, Paul (December 4, 2011). "Lloyd J. Old, Champion of Using Cells to Fight Cancer, Dies at 78". The New York Times. Retrieved 19 January 2012. 
  2. ^ Dougan, M. & Dranoff, G. (2009). Immune therapy for cancer. Annual Review of Immunology 27, 83–117
  3. ^ Old LJ, Clark DA, Benacerraf B. Effect of Bacillus Calmette Guerin infection on transplanted tumors in the mouse. Nature 1959; 184:291-292.
  4. ^ Lilly F, Boyse EA, Old LJ. Genetic basis of susceptibility to viral leukaemogenesis. Lancet. 1964 Dec 5;2(7371): 1207-9.
  5. ^ Old LJ, Boyse EA, Stockert E. Antigenic properties of experimental leukemias. I. Serological studies in vitro with spontaneous and radiation leukemies. J Natl Cancer Inst 31: 977-986.
  6. ^ Old LJ, Boyse EA, Stockert E. Typing of mouse leukemias by serological methods. Nature 1964; 201: 777-779.
  7. ^ Boyse EA, Old LJ, Luell S. Genetic determination of the TL (thymus-leukemia) antigen in the mouse. Nature 1964; 201:779.
  8. ^ Boyse EA, Miyazawa M, Aoki T, Old LJ. Ly-A and Ly-B: Two systems of lymphocyte isoantigens in the mouse. Proc R Soc Lond B Biol Sci. 1968 Jun 11; 170(19): 175-93.
  9. ^ Peter Keating and Alberto Cambrosio. Biomedical Platforms: Realigning the Normal and the Pathological in Late-Twentieth-Century Medicine. Cambridge: The MIT Press, 2003.
  10. ^ Old LJ, Boyse EA, Oettgen HF, Harven ED, Geering G, Williamson B, Clifford P. Precipitating antibody in human serum to an antigen present in cultured Burkitt's lymphoma cells. Proc Natl Acad Sci U S A. 1966 Dec;56(6):1699-704.
  11. ^ Carswell EA, Old LJ, Kassel RL, Green S, Fiore N, Williamson B. An endotoxin-induced serum factor that causes necrosis of tumors. Proc Natl Acad Sci U S A. 1975 Sep;72(9):3666-70.
  12. ^ Old LJ. Tumor necrosis factor (TNF). Science. 1985 Nov 8;230(4726):630-2.
  13. ^ DeLeo AB, Jay G, Appella E, Dubois GC, Law LW, Old LJ. 1979. Detection of a transformation-related antigen in chemically induced sarcomas and other transformed cells of the mouse. Proc Natl Acad Sci USA 76(5): 2420-4.
  14. ^ Luwor RB, Johns TG, Murone C, Huang HJ, Cavenee WK, Ritter G, Old LJ, Burgess AW, Scott AM. Monoclonal antibody 806 inhibits the growth of tumor xenografts expressing either the de2-7 or amplified epidermal growth factor receptor (EGFR) but not wild-type EGFR. Cancer Res. 2001 Jul 15;61(14):5355-61.
  15. ^ Welt S, Divgi CR, Real FX, Yeh SD, Garin-Chesa P, Finstad CL, Sakamoto J, Cohen A, Sigurdson ER, Kemeny N, Carswell EA, Oettgen HF, Old LJ. Quantitative analysis of antibody localization in human metastatic colon cancer: A phase I study with monoclonal antibody A33. J Clin Oncol 1990; 8:1894-1906.
  16. ^ Sahin U, Tureci O, Schmitt H, Cochlovius B, Johannes T, Schmits R, Stenner F, Luo G, Schobert I, Pfreundschuh M. Human neoplasms elicit multiple specific immune responses in the autologous host. Proc Natl Acad Sci USA. 1995;92:11810-11813.
  17. ^ Kaplan DH, Shankaran V, Dighe AS, Stockert E, Aguet M, Old LJ, Schreiber RD. Demonstration of an interferon gamma-dependent tumor surveillance system in immunocompetent mice. Proc Natl Acad Sci U S A. 1998 Jun 23;95(13):7556-61.
  18. ^ Shankaran V, Ikeda H, Bruce AT, White JM, Swanson PE, Old LJ, Schreiber RD. IFNgamma and lymphocytes prevent primary tumour development and shape tumour immunogenicity. Nature. 2001 Apr 26;410(6832):1107-11.
  19. ^ Dunn GP, Bruce AT, Ikeda H, Old LJ, Schreiber RD. Cancer immunoediting: from immunosurveillance to tumor escape. Nat Immunol. 2002 Nov;3(11):991-8. Review.
  20. ^ http://www.academycancerimmunology.org/index.htm

External links[edit]