Scientific Publications

Project R&R’s science team, along with other scientists, are investigating the limitations and problems of using chimpanzees as a means of studying human disease and health. They are also looking at the life-long suffering that results for chimpanzees from their use and laboratory confinement.

In the interest of open discussion, we welcome comments. If you have a paper to contribute or questions, contact: releasechimps@neavs.org

Science professionals, please Sign our Scientists Petition.

  ATLA, hep C, One

The Bioethics of Great Ape Well-Being: Psychiatric Injury and Duty of Care

Capaldo, T., Bradshaw, G.A. (2011) Animals & Society Institute Policy Paper

  folder


Lessons from Chimpanzee-Based Research on Human Disease: The Implications of Genetic Differences

Bailey, J. (2011). Alternatives to Laboratory Animals, 39(6):527–540.

  ATLA, hep C, One


An Assessment of the Use of Chimpanzees in Hepatitis C Research Past, Present and Future:
1. Validity of the Chimpanzee Model

Bailey, J. (2010). Alternatives to Laboratory Animals (ATLA), 38(5), 387-418.

Abstract

  ATLA, hep C, Two

An Assessment of the Use of Chimpanzees in Hepatitis C Research Past, Present and Future:
2. Alternative Replacement Methods

Bailey, J. (2010). Alternatives to Laboratory Animals (ATLA), 38(6), 471-494.

Abstract


  ATLA Science Paper


An Examination of Chimpanzee Use in Human Cancer Research

Bailey, J. (2009). Alternatives to Laboratory Animals (ATLA), 37(4), 399-416.

Abstract

  Science Paper


Developmental Context Effects on Bicultural Posttrauma Self Repair in Chimpanzees

Bradshaw, G.A., Capaldo, T., Lindner, L., & Grow, G. (2009). Developmental Psychology, 45(5), 1376-1388.

Abstract

  Science Paper


Building an Inner Sanctuary: Complex PTSD in Chimpanzees

Bradshaw, G.A., Capaldo, T., Lindner, L., & Grow, G. (2008). Journal of Trauma & Dissociation, 9(1), 9-34.

Abstract

  Science Paper


An Assessment of the Role of Chimpanzees in AIDS Vaccine Research

Bailey, J. (2008). Alternatives to Laboratory Animals (ATLA), 36(4), 381-428.

Abstract

  folder


Chimpanzee Research: An Examination of Its Contribution to Biomedical Knowledge and Efficacy in Combating Human Diseases and Supplement

Bailey, J., Balcombe, J. & Capaldo, T. (2007). Project R&R.

Abstract



Additional Articles and Presentations

Scientific Paper Abstracts

An Assessment of the Use of Chimpanzees in Hepatitis C Research Past, Present and Future: 1. Validity of the Chimpanzee Model

Bailey, J. (2010). Alternatives to Laboratory Animals (ATLA), 38(5), 387-418.

Full Paper

The USA is the only significant user of chimpanzees in biomedical research in the world, since many countries have banned or limited the practice due to substantial ethical, economic and scientific concerns. Advocates of chimpanzee use cite hepatitis C research as a major reason for its necessity and continuation, in spite of supporting evidence that is scant and often anecdotal. This paper examines the scientific and ethical issues surrounding chimpanzee hepatitis C research, and concludes that claims of the necessity of chimpanzees in historical and future hepatitis C research are exaggerated and unjustifiable, respectively. The chimpanzee model has several major scientific, ethical, economic and practical caveats. It has made a relatively negligible contribution to knowledge of, and tangible progress against, the hepatitis C virus compared to non-chimpanzee research, and must be considered scientifically redundant, given the array of alternative methods of inquiry now available. The continuation of chimpanzee use in hepatitis C research adversely affects scientific progress, as well as chimpanzees and humans in need of treatment. Unfounded claims of its necessity should not discourage changes in public policy regarding the use of chimpanzees in U.S. laboratories.


An Assessment of the Use of Chimpanzees in Hepatitis C Research Past, Present and Future: 2. Alternative Replacement Methods

Bailey, J. (2010). Alternatives to Laboratory Animals (ATLA), 38(6), 471-494.

Full Paper

The use of chimpanzees in hepatitis C virus (HCV) research was examined in the report associated with this paper (1: Validity of the Chimpanzee Model), in which it was concluded that claims of past necessity of chimpanzee use were exaggerated, and that claims of current and future indispensability were unjustifiable. Furthermore, given the serious scientific and ethical issues surrounding chimpanzee experimentation, it was proposed that it must now be considered redundant—particularly in light of the demonstrable contribution of alternative methods to past and current scientific progress, and the future promise that these methods hold. This paper builds on this evidence, by examining the development of alternative approaches to the investigation of HCV, and by reviewing examples of how these methods have contributed, and are continuing to contribute substantially, to progress in this field. It augments the argument against chimpanzee use by demonstrating the comprehensive nature of these methods and the valuable data they deliver. The entire life-cycle of HCV can now be investigated in a human (and much more relevant) context, without recourse to chimpanzee use. This also includes the testing of new therapies and vaccines. Consequently, there is no sound argument against the changes in public policy that propose a move away from chimpanzee use in U.S. laboratories.


An Examination of Chimpanzee Use in Human Cancer Research

Bailey, J. (2009). Alternatives to Laboratory Animals (ATLA), 37(4), 399-416.

Full Paper

Advocates of chimpanzee research claim the genetic similarity of humans and chimpanzees make them an indispensable research tool to combat human diseases. Given that cancer is a leading cause of human death worldwide, one might expect that if chimpanzees were needed for, or were productive in, cancer research, then they would have been widely used. This comprehensive literature analysis reveals that chimpanzees have scarcely been used in any form of cancer research, and that chimpanzee tumours are extremely rare and biologically different from human cancers. Often, chimpanzee citations described peripheral use of chimpanzee cells and genetic material in predominantly human genomic studies. Papers describing potential new cancer therapies noted significant concerns regarding the chimpanzee model. Other studies described interventions that have not been pursued clinically. Finally, available evidence indicates that chimpanzees are not essential in the development of therapeutic monoclonal antibodies. It would therefore be unscientific to claim that chimpanzees are vital to cancer research. On the contrary, it is reasonable to conclude that cancer research would not suffer, if the use of chimpanzees for this purpose were prohibited in the US. Genetic differences between humans and chimpanzees make them an unsuitable model for cancer, as well as other human diseases.

Developmental Context Effects on Bicultural Posttrauma Self Repair in Chimpanzees

Bradshaw, G.A., Capaldo, T., Lindner, L., & Grow, G. (2009). Developmental Psychology, 45(5), 1376-1388.

Full Paper

Longitudinal studies have shown how early developmental contexts contribute significantly to self-development; their influence extends through adulthood, informs sociality, and affects resilience under severe stress. While the importance of sociality in trauma recovery is recognized, the relationship between developmental and posttrauma contexts and recovery effects is less appreciated, particularly in cases in which recovery contexts differ widely from the culture of origin. Using an attachment-based model of bicultural (competence in two cultures) development, the authors examined the role of self in posttrauma repair of chimpanzees (Pan troglodytes) who had been differentially reared by humans during neuroethologically formative periods and subsequently used as biomedical subjects. Results show that variations in posttrauma schema correlate with early socialization patterns. Self-resilience supports, but also may constrain, recovery depending on the compatibility of internal self models with recovery resources. Trauma severity notwithstanding, the cultural context of origin emerges as a critical factor in designing effective therapeutic intervention and assessments in primates, humans inclusive. Finally, the results underscore the ethical implications for the practices of cross-fostering nonhuman primates and their use in research.

Building an Inner Sanctuary: Complex PTSD in Chimpanzees

Bradshaw, G.A., Capaldo, T., Lindner, L., & Grow, G. (2008). Journal of Trauma & Dissociation, 9(1), 9-34.

Full Paper

Through the analysis of case studies of chimpanzees (Pan troglodytes) in residence at a sanctuary, who previously sustained prolonged captivity and biomedical experimentation, we illustrate how human psychological models of diagnosis and treatment might be approached in great apes. This study reflects growing attention to ethical, scientific, and practical problems associated with psychological well-being of animals. The analysis concludes that a diagnosis of Complex PTSD in chimpanzees is consistent with descriptions of trauma-induced symptoms as described by the DSM-IV and human trauma research. We report on how these findings contribute to diagnosis and treatment of chimpanzees in captivity and elucidate discussion concerning their continued laboratory use. This clinical study contributes toward theory and therapeutic practices of an emergent trans-species psychology inclusive of both humans and other species. Such an ability to extend what we know about models of human trauma opens deeper understanding and insights into ourselves as well as individuals from other species.

An Assessment of the Role of Chimpanzees in AIDS Vaccine Research

Bailey, J. (2008). Alternatives to Laboratory Animals (ATLA), 36(4), 381-428.

Full Paper

Prior to Simian Immunodeficiency Virus (SIV)-infected macaques becoming the ‘model of choice’ in the 1990s, chimpanzees were widely used in AIDS vaccine research and testing. Faced with the continued failure to develop an effective human vaccine, some scientists are calling for a return to their widespread use. To assess the past and potential future contribution of chimpanzees to AIDS vaccine development, databases and published literature were systematically searched to compare the results of AIDS vaccine trials in chimpanzees with those of human clinical trials, and to determine whether the chimpanzee trials were predictive of the human response. Protective and/or therapeutic responses have been elicited in chimpanzees, via: passive antibody transfer; CD4 analogues; attenuated virus; many types and combinations of recombinant HIV proteins; DNA vaccines; recombinant adenovirus and canarypox vaccines; and many multi-component vaccines using more than one of these approaches. Immunogenicity has also been shown in chimpanzees for vaccinia-based and peptide vaccines. Protection and/or significant therapeutic effects have not been demonstrated by any vaccine to date in humans. Vaccine responses in chimpanzees and humans are highly discordant. Claims of the importance of chimpanzees in AIDS vaccine development are without foundation, and a return to the use of chimpanzees in AIDS research/vaccine development is scientifically unjustifiable.

Chimpanzee Research: An Examination of Its Contribution to Biomedical Knowledge and Efficacy in Combating Human Diseases

Bailey, J., Balcombe, J. & Capaldo, T. (2007). Project R&R.

Full Paper

Research on captive chimpanzees (Pan troglodytes) incurs considerable animal welfare, ethical and financial costs. Advocates of such research claim these costs are outweighed by substantial advancements in biomedical knowledge, and that the genetic similarity of chimpanzees to humans enables the former to make critical contributions to preventing, diagnosing and combating human diseases. To assess these claims, we examined the disciplines investigated in 749 studies of captive chimpanzees published from 1995 – 2004 inclusive, and subjected 95 randomly selected papers to a detailed citation analysis: 49.5% (47/95) of papers had not been cited at the time of this study; 38.5% (34/95) were cited by 116 papers that did not describe well-developed methods for combating human diseases; 14.7% (14/95) of these chimpanzee studies were cited by (a total of 27) papers describing well-developed prophylactic, diagnostic or therapeutic methods for combating human diseases. Close examination of these 27 human medical papers revealed that in vitro research, human clinical and epidemiological investigations, molecular assays and methods, and genomic studies, contributed most to their development. Duplication of human outcomes, inconsistency with other human or primate data, and other causes resulted in the absence of any chimpanzee study demonstrating an essential contribution, or, in most cases, even a significant contribution of any kind, towards the development of the described human treatment.

Senate Cosponsors of the Great Ape Protection and Cost Savings Act (S.810)

15 Senate Cosponsors (S.810)

If your Senators are not listed please sign our automated letter.

Alabama

Alaska
Sen Begich, Mark [AK]—11/18/2011

Arizona

Arkansas

California

Colorado

*Connecticut
Sen Blumenthal, Richard [CT]—10/17/2011
Sen Lieberman, Joseph I. [CT]—4/13/2011

Delaware

Florida

Georgia

Hawaii
Sen Akaka, Daniel K. [HI]—7/20/2011
Sen Inouye, Daniel K. [HI]—1/26/2012

Idaho
Illinois

Indiana

Iowa

Kansas

Kentucky

Louisiana

Maine
Sen Collins, Susan M. [ME]—4/13/2011

Maryland

Massachusetts
Sen Kerry, John F. [MA]—10/11/2011

Michigan

Minnesota

Mississippi

Missouri

Montana

Nebraska

Nevada

New Hampshire

New Jersey
Sen Menendez, Robert [NJ]—2/16/2012

New Mexico
Sen Udall, Tom [NM]—12/15/2011

New York
Sen Gillibrand, Kirsten E. [NY]—10/3/2011

North Carolina

North Dakota

Ohio
Sen Brown, Sherrod [OH]—6/9/2011

Oklahoma

Oregon
Sen Merkley, Jeff [OR]—11/18/2011

Pennsylvania

Rhode Island

South Carolina

South Dakota

Tennessee

Texas

Utah

*Vermont
Sen Leahy, Patrick J. [VT]—12/1/2011
Sen Sanders, Bernard [VT]—4/13/2011

Virginia

Washington
Sen Cantwell, Maria [WA] (introduced 4/13/2011)

West Virginia

Wisconsin

Wyoming

*All Reps and Senators are now signed on for this state.

House Cosponsors of the Great Ape Protection and Cost Savings Act (H.R.1513)

162 House Cosponsors of H.R.1513

If your Rep is not listed below please sign our automated letter.

Alabama

Alaska

American Samoa

Arizona
Rep Grijalva, Raul M. [AZ-7]—6/3/2011

Arkansas

California
Rep Baca, Joe [CA-43]—1/27/2012
Rep Becerra, Xavier [CA-31]—12/13/2011
Rep Berman, Howard L. [CA-28]—6/3/2011
Rep Bono Mack, Mary [CA-45]—4/13/2011
Rep Calvert, Ken [CA-44]—12/19/2011
Rep Campbell, John [CA-48]—4/13/2011
Rep Capps, Lois [CA-23]—10/12/2011
Rep Chu, Judy [CA-32]—7/14/2011
Rep Davis, Susan A. [CA-53]—11/29/2011
Rep Farr, Sam [CA-17]—11/18/2011
Rep Filner, Bob [CA-51]—4/13/2011
Rep Hahn, Janice [CA-36]—9/2/2011
Rep Lee, Barbara [CA-9]—6/3/2011
Rep Lofgren, Zoe [CA-16]—9/2/2011
Rep Matsui, Doris O. [CA-5]—12/1/2011
Rep McNerney, Jerry [CA-11]—5/4/2011
Rep Miller, George [CA-7]—4/13/2011
Rep Napolitano, Grace F. [CA-38]—5/4/2011
Rep Richardson, Laura [CA-37]—4/13/2011
Rep Rohrabacher, Dana [CA-46]— 2/15/2012
Rep Roybal-Allard, Lucille [CA-34]—11/16/2011
Rep Sanchez, Linda T. [CA-39]—12/16/2011
Rep Sanchez, Loretta [CA-47]—12/13/2011
Rep Schiff, Adam B. [CA-29]—6/3/2011
Rep Sherman, Brad [CA-27]—4/13/2011
Rep Speier, Jackie [CA-12]—12/16/2011
Rep Stark, Fortney Pete [CA-13]—4/13/2011
Rep Woolsey, Lynn C. [CA-6]—4/13/2011

Colorado
Rep Polis, Jared [CO-2]—10/4/2011

*Connecticut
Rep Courtney, Joe [CT-2]—4/13/2011
Rep DeLauro, Rosa L. [CT-3]—5/4/2011
Rep Himes, James A. [CT-4]—9/2/2011
Rep Larson, John B. [CT-1]—7/20/2011
Rep Murphy, Christopher S. [CT-5]—4/13/2011

Delaware
Rep Carney, John [DE]—12/20/2011

Washington, D.C.
Rep Norton, Eleanor Holmes [DC]—4/13/2011

Florida
Rep Buchanan, Vern [FL-13] - 12/13/2011
Rep Castor, Kathy [FL-11]—9/2/2011
Rep Hastings, Alcee L. [FL-23]—7/14/2011
Rep Wasserman Schultz, Debbie [FL-20]—9/2/2011
Rep West, Allen B. [FL-22]—11/3/2011
Rep Wilson, Frederica [FL-17]—1/27/2012
Rep Young, C.W. Bill [FL-10]—4/13/2011

Georgia
Rep Gingrey, Phil [GA-11]—2/15/2012
Rep Johnson, Henry C. “Hank,” Jr. [GA-4]—4/13/2011
Rep Kingston, Jack [GA-1]—2/15/2012

Guam
Rep Bordallo, Madeleine Z. [GU]—4/13/2011

Hawaii
Rep Hanabusa, Colleen W. [HI-1]—11/16/2011
Rep Hirono, Mazie K. [HI-2]—12/15/2011

Idaho

Illinois
Rep Costello, Jerry F. [IL-12]—12/23/2011
Rep Davis, Danny K. [IL-7]—11/29/2011
Rep Gutierrez, Luis V. [IL-4]—7/14/2011
Rep Jackson, Jesse L., Jr. [IL-2]—12/19/2011
Rep Johnson, Timothy V. [IL-15]—11/16/2011
Rep Quigley, Mike [IL-5]—4/13/2011
Rep Schakowsky, Janice D. [IL-9]—4/13/2011
Rep Schock, Aaron [IL-18]—12/19/2011

Indiana
Rep Carson, Andre [IN-7]—4/13/2011

Iowa
Rep Braley, Bruce L. [IA-1]—6/3/2011

Kansas

Kentucky
Rep Whitfield, Ed [KY-1]—6/16/2011
Rep Yarmuth, John A. [KY-3]—12/13/2011

Louisiana

Maine
Rep Michaud, Michael H. [ME-2]—12/13/2011
Rep Pingree, Chellie [ME-1]—12/15/2011

Maryland
Rep Bartlett, Roscoe G. [MD-6] (introduced 4/13/2011)
Rep Cummings, Elijah E. [MD-7]—12/15/2011
Rep Edwards, Donna F. [MD-4]—12/19/2011
Rep Ruppersberger, C. A. Dutch [MD-2]—12/20/2011
Rep Sarbanes, John P. [MD-3]—4/13/2011
Rep Van Hollen, Chris [MD-8]—4/13/2011

Massachusetts
Rep Capuano, Michael E. [MA-8]—9/2/2011
Rep Lynch, Stephen F. [MA-9]—11/3/2011
Rep Markey, Edward J. [MA-7]—12/13/2011
Rep McGovern, James P. [MA-3]—10/13/2011
Rep Neal, Richard E. [MA-2]—10/12/2011
Rep Olver, John W. [MA-1]—11/3/2011
Rep Tierney, John F. [MA-6]—6/3/2011
Rep Tsongas, Niki [MA-5]—11/3/2011

Michigan
Rep Clarke, Hansen [MI-13]—12/15/2011
Rep Conyers, John, Jr. [MI-14]—10/5/2011
Rep Kildee, Dale E. [MI-5]—6/16/2011
Rep McCotter, Thaddeus G. [MI-11]—12/16/2011
Rep Peters, Gary C. [MI-9]—4/13/2011
Rep Walberg, Tim [MI-7]—11/18/2011

Minnesota
Rep Ellison, Keith [MN-5]—4/13/2011
Rep McCollum, Betty [MN-4]—4/13/2011

Mississippi

Missouri
Rep Carnahan, Russ [MO-3]—1/27/2012
Rep Clay, Wm. Lacy [MO-1]—11/15/2011
Rep Cleaver, Emanuel [MO-5]—12/13/2011

Montana

Nebraska

Nevada
Rep Berkley, Shelley [NV-1]—10/12/2011

New Hampshire
Rep Bass, Charles F. [NH-2]—12/1/2011

New Jersey
Rep Andrews, Robert E. [NJ-1]—4/13/2011
Rep Holt, Rush D. [NJ-12]—6/16/2011
Rep Lance, Leonard [NJ-7]—11/29/2011
Rep LoBiondo, Frank A. [NJ-2]—11/15/2011
Rep Pascrell, Bill, Jr. [NJ-8]—6/3/2011
Rep Payne, Donald M. [NJ-10]—11/29/2011
Rep Rothman, Steven R. [NJ-9]—4/13/2011
Rep Sires, Albio [NJ-13]—1/27/2012
Rep Smith, Christopher H. [NJ-4]—4/13/2011

New Mexico
Rep Heinrich, Martin [NM-1]—4/13/2011
Rep Lujan, Ben Ray [NM-3]—4/13/2011

New York
Rep Ackerman, Gary L. [NY-5]—4/13/2011
Rep Bishop, Timothy H. [NY-1]—12/19/2011
Rep Crowley, Joseph [NY-7]—11/3/2011
Rep Grimm, Michael G. [NY-13]—7/14/2011
Rep Hanna, Richard L. [NY-24]—11/15/2011
Rep Hayworth, Nan A. S. [NY-19]—12/16/2011
Rep Hinchey, Maurice D. [NY-22]—4/13/2011
Rep Israel, Steve [NY-2]—4/13/2011
Rep King, Peter T. [NY-3]—12/1/2011
Rep Lowey, Nita M. [NY-18]—5/4/2011
Rep Maloney, Carolyn B. [NY-14]—6/3/2011
Rep McCarthy, Carolyn [NY-4]—5/4/2011
Rep Meeks, Gregory W. [NY-6]—12/15/2011
Rep Nadler, Jerrold [NY-8]—4/13/2011
Rep Owens, William L. [NY-23]—6/16/2011
Rep Rangel, Charles B. [NY-15]—4/13/2011
Rep Serrano, Jose E. [NY-16]—11/3/2011
Rep Slaughter, Louise McIntosh [NY-28]—12/15/2011
Rep Tonko, Paul [NY-21]—5/4/2011
Rep Towns, Edolphus [NY-10]—4/13/2011
Rep Velazquez, Nydia M. [NY-12]—11/3/2011
Rep Weiner, Anthony D. [NY-9]—5/4/2011

North Carolina
Rep Jones, Walter B., Jr. [NC-3]—2/15/2012
Rep Kissell, Larry [NC-8]—4/13/2011
Rep Myrick, Sue Wilkins [NC-9]—2/15/2012
Rep Price, David E. [NC-4]—11/15/2011
Rep Shuler, Heath [NC-11]—12/23/2011

North Dakota

Northern Mariana Islands
Rep Sablan, Gregorio Kilili Camacho [MP]—2/15/2012

Ohio
Rep Kaptur, Marcy [OH-9]—4/13/2011
Rep Kucinich, Dennis J. [OH-10]—10/13/2011
Rep LaTourette, Steven C. [OH-14]—10/27/2011
Rep Sutton, Betty [OH-13]—4/13/2011

Oklahoma

Oregon
Rep Blumenauer, Earl [OR-3]—10/12/2011
Rep DeFazio, Peter A. [OR-4]—4/13/2011

Pennsylvania
Rep Brady, Robert A. [PA-1]—4/13/2011
Rep Critz, Mark S. [PA-12]—6/14/2011
Rep Doyle, Michael F. [PA-14]—11/29/2011
Rep Fitzpatrick, Michael G. [PA-8]—11/15/2011
Rep Gerlach, Jim [PA-6]—4/13/2011
Rep Marino, Tom [PA-10]—11/3/2011

Puerto Rico

Rhode Island
Rep Cicilline, David N. [RI-1]—11/3/2011
Rep Langevin, James R. [RI-2]—4/13/2011

South Carolina

South Dakota

Tennessee
Rep Cohen, Steve [TN-9]—11/15/2011
Rep Duncan, John J., Jr. [TN-2]—2/15/2012

Texas
Rep Jackson Lee, Sheila [TX-18]—12/19/2011
Rep Johnson, Eddie Bernice [TX-30]—12/16/2011
Rep Reyes, Silvestre [TX-16]—10/5/2011

Utah

*Vermont
Rep Welch, Peter [VT]—11/29/2011

Virgin Islands of the United States

Virginia
Rep Connolly, Gerald E. “Gerry” [VA-11]—7/20/2011
Rep Moran, James P. [VA-8]—4/13/2011
Rep Scott, Robert C. “Bobby” [VA-3]—12/13/2011

Washington
Rep Dicks, Norman D. [WA-6]—11/3/2011
Rep Inslee, Jay [WA-1]—9/2/2011
Rep McDermott, Jim [WA-7]—11/16/2011
Rep Reichert, David G. [WA-8]—4/13/2011

West Virginia
Rep Rahall, Nick J., II [WV-3]—11/18/2011

Wisconsin
Rep Moore, Gwen [WI-4]—5/4/2011

Wyoming

*All Reps and Senators are now signed on for this state.



Please bookmark with social media, your votes are noticed and appreciated:



back to top