Court of Appeals for the Fourth Circuit
Estate of Arturo Giron Alvarez v. Rockefeller Foundation
22-16781 citation·
Summary of the case Estate of Arturo Giron Alvarez v. Rockefeller Foundation
The case involves a class of 842 plaintiffs who brought claims under the Alien Tort Statute against The Rockefeller Foundation (TRF) for its alleged involvement in nonconsensual human medical experiments in Guatemala from 1946 to 1948. The district court granted summary judgment in favor of TRF, finding that TRF was not liable as a principal under the ATS because Dr. Frederick Soper, involved in the experiments, was not acting as an agent of TRF. The Fourth Circuit affirmed the district court's decision.
Key Issues of the case Estate of Arturo Giron Alvarez v. Rockefeller Foundation
- Whether TRF can be held liable under the ATS for the actions of Dr. Soper in the Guatemala Experiments
- Whether Dr. Soper was acting as an agent of TRF during the experiments
Key Facts of the case Estate of Arturo Giron Alvarez v. Rockefeller Foundation
- The Guatemala Experiments involved nonconsensual infection of individuals with STDs.
- Dr. Soper was assigned to the Pan-American Sanitary Bureau and not under TRF's control during the experiments.
Decision of the case Estate of Arturo Giron Alvarez v. Rockefeller Foundation
Affirmed
Impact of the case Estate of Arturo Giron Alvarez v. Rockefeller Foundation
The decision limits the liability of organizations for the actions of individuals not acting under their control.
Opinions
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PUBLISHED
UNITED STATES COURT OF APPEALS
FOR THE FOURTH CIRCUIT
No. 22-1678
ESTATE OF ARTURO GIRON ALVAREZ, by and through Maria Ana Giron
Galindo as Administrator; THE 773 INDIVIDUALS IDENTIFIED ON EXHIBIT
1 TO THE COMPLAINT; UNKNOWN USE PLAINTIFFS,
Plaintiffs – Appellants,
v.
THE ROCKEFELLER FOUNDATION,
Defendant – Appellee.
Appeal from the United States District Court for the District of Maryland, at Baltimore.
Theodore D. Chuang, District Judge. (1:15-cv-00950-TDC)
Argued: December 7, 2023 Decided: March 20, 2024
Before WILKINSON and HEYTENS, Circuit Judges, and Henry E. HUDSON, Senior
United States District Judge for the Eastern District of Virginia, sitting by designation.
Affirmed by published opinion. Judge Hudson wrote the opinion, in which Judge
Wilkinson and Judge Heytens joined. Judge Wilkinson wrote a concurring opinion.
ARGUED: Paul David Bekman, BEKMAN, MARDER, HOPPER, MALARKEY &
PERLIN, L.L.C., Baltimore, Maryland; Floyd Ronald Jenkins, MERIDIAN 361
INTERNATIONAL LAW GROUP PLLC, Portland, Maine, for Appellants. Michael
Hugh McGinley, DECHERT LLP, Philadelphia, Pennsylvania, for Appellee. ON BRIEF:
Sheila L. Birnbaum, Danielle A. Gentin Stock, DECHERT LLP, New York, New York;
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Robert P. LoBue, David S. Kleban, PATTERSON BELKNAP WEBB & TYLER LLP,
New York, New York; Jim Frederick, FAEGRE DRINKER, Washington, D.C., for
Appellee.
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HUDSON, District Judge:
This matter is before the Court on serious deprivations and violations of human
rights. A class of 842 plaintiffs brought claims under the Alien Tort Statute (“ATS”) and
the Guatemalan Civil Code against Johns Hopkins, The Rockefeller Foundation (“TRF”),
and Bristol-Myers Squibb Company (“Bristol-Myers”), alleging that the defendants were
involved in facilitating nonconsensual human medical experiments regarding sexually
transmitted diseases (“STDs”) in Guatemala from 1946 to 1948 (the “Guatemala
Experiments” or “Experiments”). The defendants filed a motion for summary judgment,
and the district court granted the motion. The plaintiffs filed this appeal, only challenging
the district court’s order granting summary judgment in relation to the defendant, TRF. For
the following reasons, we affirm.
I
In reviewing the district court’s grant of summary judgment, we view the facts in
the light most favorable to Appellants. Estate of Jones v. City of Martinsburg, 961 F.3d
661, 664 (4th Cir. 2020). This appeal concerns 842 victims 1 (collectively, “Appellants”) of
1
The 842 plaintiffs are comprised of six categories: (1) individuals who were
unknowingly infected with syphilis and did not consent to being infected (collectively,
“Direct Plaintiffs”); (2) spouses or sexual partners of Direct Plaintiffs subjected to
secondary exposure to syphilis; (3) children of Direct Plaintiffs subjected to secondary
exposure to syphilis passed in utero or at birth; (4) grandchildren of Direct Plaintiffs
subjected to secondary exposure to syphilis across two generations; (5) parents, spouses,
or children of individuals who died as a result of syphilis acquired from the Guatemala
Experiments; and (6) the estates and designated beneficiaries of those who died as a result
of syphilis.
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the Guatemala Experiments—a horrific set of unethical and inhumane experiments
conducted on human test subjects in Guatemala to study STDs.
In the 1940s, the United States grew concerned with the heightened outbreaks of
STDs—particularly, gonorrhea and syphilis. Thus, Dr. Juan Funes (“Dr. Funes”), a
Guatemalan physician who previously conducted STD experiments, proposed a research
project in Guatemala to study methods of prophylaxis 2 for syphilis. Because commercial
sex work was legal in Guatemala, Dr. Funes’ proposed identifying inmate volunteers at a
Guatemalan prison, exposing them to STDs through sexual intercourse with infected sex
workers, and then testing the effectiveness of a specific prophylaxis on the inmate
volunteers. This proposal created the infamous Guatemala Experiments.
In 1946, Dr. Thomas Parran (“Dr. Parran”), the Surgeon General of the United
States Public Health Service (the “PHS”), 3 approved Dr. Funes’ proposal and
recommended the project to the National Advisory Health Council (the “NAHC”) for
funding. The NAHC recommended funding the proposal, and the grant was ultimately
approved, including $110,450 to be provided to the Pan-American Sanitary Bureau
(“PASB”) for venereal disease studies in Guatemala. The Venereal Disease Research
Laboratory (“VDRL”), a subsect of the PHS, directly funded the Guatemala Experiments.
2
Prophylaxis is a method to prevent the spread of syphilis.
3
Dr. Parran simultaneously served as a member of TRF’s Board of Trustees and of
the Board of Scientific Directors of TRF’s International Health Division (“IHD”).
4
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After completion of the laboratory in Guatemala, serology testing 4 began at the
prison in November 1946. In February 1947, Dr. John C. Cutler (“Dr. Cutler”), a junior
PHS officer, and his research team began infecting test subjects with STDs as part of the
study. The researchers infected prisoners by arranging sexual intercourse between the
volunteer prisoners and commercial sex workers (referred to as “normal exposure”), or by
injecting or directly applying the STD to the test subject. There are no records indicating
that the sex workers were compensated. From May 1947 to October 1948, the researchers
conducted thirty-two (32) experiments using gonorrhea, seventeen (17) using syphilis, and
one (1) using chancroid, which, collectively, involved a total of 1,308 people, ranging from
ten (10) to seventy-two (72) years old.
The method of normal exposure proved to be ineffective in transferring syphilis and
its symptoms of infection to the prisoners. This ineffectiveness led researchers to directly
inject syphilitic materials into the prisoner test subjects. From May 1947 to September
1948, 219 prisoners were exposed to syphilis either by sex workers or direct injection, and
only ninety-two (92) received some form of treatment. There is no contemporaneous record
of the prisoners consenting to their participation in the Guatemala Experiments. Nor are
there records indicating that the prisons knew or understood that the Guatemala
Experiments were ongoing.
4
Serology testing is a procedure that tests blood for the presence of syphilis
antibodies in order to reliably diagnose active or previous syphilitic infection.
5
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Because of the obstacles the researchers faced at the prison, Dr. Cutler
recommended conducting experiments on patients at the Guatemalan psychiatric hospital.
These experiments occurred from May 1947 to October 1948. Patients were exposed to
syphilis by injection or direct application of a cotton ball moistened with syphilitic
material. When these methods proved ineffective, Dr. Cutler began infecting patients
through scarification and abrasions on their genitals—a gruesome and drastic tactic of
infection. Patients were also infected by oral ingestion of syphilitic material and through
cisternal punctures, where syphilis was directly injected into their spinal fluid from the
back of the skull.
The psychiatric test patients were not paid for their participation in these
experiments. Instead, Dr. Cutler gave them cigarettes and purchased items for the benefit
of the psychiatric hospital. Like with the prisoner test subjects, there is no evidence that
the psychiatric patients consented to the experiments, nor is there evidence that they knew
or understood that the Guatemala Experiments were ongoing. However, there is evidence
that patients actively objected to the experiments.
Dr. Cutler and his team also conducted experiments to research gonorrhea, which
ran concurrently with the syphilis experiments. In these experiments, members of the
Guatemalan Army were exposed to gonorrhea through sexual intercourse with commercial
sex workers. Similarly, there is no evidence that the soldiers consented or were
compensated for their participation.
After experiencing issues recruiting sex workers who were willing to participate in
the gonorrhea experiments, the researchers began directly infecting sex workers with
6
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gonorrhea by applying a cotton swab moistened with gonorrhea to the cervix. Again, there
is no evidence that the sex workers consented, nor is there evidence that they were aware
they were being infected with gonorrhea. When these methods proved ineffective, the
researchers began directly injecting gonorrhea into the sex workers and psychiatric patients
through inoculation in the rectum, urethra, or eyes.
Throughout these experiments, Dr. Cutler and his research team continued to engage
in serology testing. This testing involved blood tests and lumbar punctures to evaluate
whether the human test subjects had active or previous infections from STDs. The serology
testing originally occurred only on the Guatemalan prisoners, soldiers, and psychiatric
patients. However, it was later administered on patients at the Venereal Disease and Sexual
Prophylaxis Hospital, patients at a leprosy facility, and children. 5
The Guatemala Experiments’ funding ran through June 1948, but serology testing
continued until at least 1949, and the observation and study of human test subjects at the
psychiatric hospital continued until at least 1953.
II
TRF is a foundation involved in national and international research in public health
and, during the mid-1900s, had a particular interest in discovering a cure for syphilis. The
IHD was TRF’s sole operating division, and was led by a Director and Associate Directors,
who served as officers of TRF. The IHD assigned its personnel to “work through official
5
The serology testing on children occurred from approximately June 1947 to the
summer of 1949. The researchers conducted testing on 1,384 children between the ages of
one (1) and eighteen (18).
7
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government agencies.” J.A. 821. The Director of the IHD, Dr. George Strode (“Dr.
Strode”), assigned Dr. Frederick Soper (“Dr. Soper”), an Associate Director of TRF, to the
PASB in February 1947, coinciding with the Guatemala Experiments. Dr. Strode informed
Dr. Soper that this was a “change of assignment.” J.A. 1014. However, Dr. Soper believed
that he was no longer a part of TRF. See J.A. 2542 (After assuming his position with the
PASB, Dr. Soper wrote that he “ha[d] three organizations to serve, the World Health
Organization, the Pan American Sanitary Bureau[,] and the Pan American Union.”);
J.A. 1009 (Dr. Soper indicated that he “was no longer with the Foundation, but with the
Pan American Health Organization . . . .”).
While assigned to the PASB, Dr. Soper remained an Associate Director of IHD, and
TRF continued to pay his salary and benefits until January 1, 1948. At this time, the PASB
was financially unstable, and functioned with a limited budget and operational funds.
Notably, the PASB’s constitution, approved in January 1947 and formally adopted in
October 1947, prohibited Dr. Soper, and all PASB personnel, from “seek[ing] []or
receiv[ing] instructions from any government or from any authority external to the Pan
American Sanitary Organization.” J.A. 1930.
While Dr. Soper served the PASB, the NAHC re-authorized funding for the
Guatemala Experiments. This funding was designated for the PASB, where Dr. Soper
served as the “Investigator” for the Experiments. J.A. 1307. As Investigator, Dr. Soper kept
a journal detailing the Guatemala Experiments—including his accounts of the artificial
inoculation of syphilis and gonorrhea in human test subjects and the results of the serology
testing.
8
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III
Prior to the case at hand, a class of victims of the Guatemala Experiments, and their
heirs, filed suit in the United States District Court for the District of Columbia against the
Secretary of Health and Human Services, the Surgeon General of the PHS, the Director of
the Pan-American Health Organization, 6 and other federal officials. The class action sought
to hold the defendants liable for the Guatemala Experiments under the ATS and the United
States Constitution. See Garcia v. Sebelius, 867 F. Supp. 2d 125, 130–31 (D.D.C. 2012),
vacated in part, 919 F. Supp. 2d 43 (D.D.C. 2013). The district court ultimately dismissed
the case, concluding that the United States had not waived sovereign immunity for the tort
claims, the plaintiffs failed to allege the requisite personal involvement necessary to
maintain the constitutional claims, and the Pan-American Health Organization was entitled
to immunity under the International Organizations Immunities Act of 1945. Id. at 137–38,
144.
Appellants filed the present lawsuit in the United States District Court for the
District of Maryland on April 1, 2015. They asserted claims under the ATS and the
Guatemalan Civil Code against Johns Hopkins, TRF, and Bristol-Myers, alleging that
“physicians, researchers, and other employees and agents” of the defendants “designed,
developed, approved, encouraged, directed, oversaw, and aided and abetted
nonconsensual, nontherapeutic, human subject experiments in Guatemala . . . .” J.A. 55.
Bristol-Myers was subsequently voluntarily dismissed as a defendant.
6
The Pan-American Health Organization is the successor organization to the PASB.
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In 2017, the district court dismissed all claims under the Guatemalan Civil Code.
The court also dismissed the ATS claims based on direct liability, except for a limited claim
against TRF. However, the court declined to dismiss plaintiffs’ ATS claims based on aiding
and abetting and conspiracy liability.
As to the remaining claims, the operative complaint alleged that a group of
researchers at Johns Hopkins and TRF, who spent their careers studying syphilis,
“intentionally chose to conduct nontherapeutic, nonconsensual experiments because doing
so allowed them to quickly identify a large pool of uninfected people, infect them with
syphilis strains, . . . and then use the newly infected men and women as a resource to be
consumed as a means to their ends” of advancing their research interests. J.A. 56.
Additionally, they alleged that TRF “actively participated in, joined and participated in a
conspiracy to further, and aided and abetted the Guatemala Experiments” through essential
personnel, namely, Dr. Parran and Dr. Soper. J.A. 127.
The parties filed cross-motions for summary judgment on these claims. The district
court granted TRF’s motion on the ground that Dr. Parran and Dr. Soper were not acting
as agents of TRF, and, therefore, TRF is not liable as a principal under the ATS. Appellants
now appeal to this Court the district court’s grant of TRF’s motion for summary judgment
as it relates to Dr. Soper.
IV
On appeal, Appellants argue that the district court erred when it granted TRF
summary judgment. “We review de novo a district court’s decision to grant summary
judgment, applying the same legal standards as the district court and viewing all facts and
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reasonable inferences in the light most favorable to the nonmoving party.” Ballengee v.
CBS Broad., Inc., 968 F.3d 344, 349 (4th Cir. 2020). Summary judgment is proper only “if
the movant shows that there is no genuine dispute as to any material fact and the movant
is entitled to judgment as a matter of law.” FED. R. CIV. P 56(a). To create a genuine issue
of material fact, the nonmoving party must offer “‘sufficient proof in the form of admissible
evidence’ instead of ‘relying solely on the allegations of her pleadings.’” Webster v.
Chesterfield Cnty. Sch. Bd., 38 F.4th 404, 410 (4th Cir. 2022) (quoting Guessous v.
Fairview Prop. Invs., LLC, 828 F.3d 208, 216 (4th Cir. 2016)). However, “the nonmoving
party must rely on more than conclusory allegations, mere speculation, the building of one
inference upon another, or the mere existence of a scintilla of evidence.” Humphreys &
Partners Architects v. Lessard Design, Inc., 790 F.3d 532, 540 (4th Cir. 2015) (quoting
Dash v. Mayweather, 731 F.3d 303, 311 (4th Cir. 2013)) (internal quotation marks
omitted). “[T]he relevant inquiry is ‘whether the evidence presents a sufficient
disagreement to require submission to a jury or whether it is so one-sided that one party
must prevail as a matter of law.’” Gordon v. Schilling, 937 F.3d 348, 356 (4th Cir. 2019)
(quoting Anderson v. Liberty Lobby, Inc., 477 U.S. 242, 251–52 (1986)).
To establish aiding and abetting liability in an ATS claim, Appellants must show
that a defendant “(1) provide[d] practical assistance to the principal which has a substantial
effect on the perpetration of the crime, and (2) [did] so with the purpose of facilitating the
commission of that crime.” Aziz v. Alcolac, Inc., 658 F.3d 388, 396 (4th Cir. 2011) (quoting
Presbyterian Church of Sudan v. Talisman Energy, Inc., 582 F.3d 244, 258 (2d Cir. 2009))
(internal quotations omitted). Additionally, this Court has held that “for liability to attach
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under the ATS for aiding and abetting a violation of international law, a defendant must
provide substantial assistance with the purpose of facilitating the alleged violation.” Id. at
401. Knowledge alone is not enough to establish liability. Id. (“[N]o . . . consensus exists
for imposing liability on [those] who knowingly (but not purposefully) aid and abet a
violation of international law.” (quoting Talisman, 582 F.3d at 259) (internal quotations
omitted) (modifications in original)).
“Under traditional agency law, an agency relationship exists when a principal
‘manifests assent’ to an agent ‘that the agent shall act on the principal’s behalf and subject
to the principal’s control, and the agent manifests assent or otherwise consents so to act.’”
Krakauer v. Dish Network, L.L.C., 925 F.3d 643, 659–60 (4th Cir. 2019) (quoting
RESTATEMENT (THIRD) OF AGENCY § 1.01 (AM. L. INST. 2006)). “Agencies . . . come in
many sizes and shapes: One may be an agent for some business purposes and not others so
that the fact that one may be an agent for one purpose does not make him or her an agent
for every purpose.” Daimler AG v. Bauman, 571 U.S. 117, 135 (2014) (internal quotations
and citation omitted).
A principal is only liable for an agent’s tortious acts if the acts were performed
within the scope of employment, which is conduct “of the same general nature as that
authorized, or incidental to the conduct authorized.” RESTATEMENT (SECOND) OF AGENCY
§§ 219, 229 (AM. L. INST. 1957). It is possible for an individual to be the agent of two
principals at the same time. See N.L.R.B. v. Town & Country Elec., Inc., 516 U.S. 85, 94–
95 (1995) (“[A] person may be the servant of two masters . . . at one time as to one act, if
the service to one does not involve abandonment of the service to the other.” (quoting
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RESTATEMENT (SECOND) OF AGENCY § 226 (AM. LAW. INST. 1957)) (emphasis omitted)).
This can occur when an agent is “lent,” i.e., where he is “in the general service of [a
principal], and, nevertheless, with respect to particular work, may be transferred, with his
own consent or acquiescence, to the service of a third person, so that he becomes the servant
of that person, with all the legal consequences of the new relation.” Standard Oil Co. v.
Anderson, 212 U.S. 215, 220 (1909); see also Ladd v. Rsch. Triangle Inst., 335 F. App’x
285, 288 (4th Cir. 2009) (“A person can be in the general employ of one company while at
the same time being in the particular employ of another . . . .”).
When determining whether such a transfer has occurred, “we must inquire whose is
the work being performed;” this question “is usually answered by ascertaining who has the
power to control and direct the servants in the performance of their work.” Standard Oil,
212 U.S. at 221–22; see also RESTATEMENT (SECOND) OF AGENCY § 227 cmt. a (AM. LAW
INST. 1957) (“[T]he important question is not whether or not [the agent] remains the servant
of the general employer as to matters generally, but whether or not, as to the act in question,
he is acting in the business of and under the direction of one or the other.”). When an agent
has been lent by one principal to the service of another, the agent, “in respect of his acts in
that service, is to be dealt with as the servant of the latter and not of the former.” Denton v.
Yazoo & M.V.R. Co., 284 U.S. 305, 308 (1932).
V
In applying the aforementioned standards, this Court finds that the district court did
not err in granting summary judgment to TRF. Appellants argue that the evidence
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demonstrates Dr. Soper was an agent of TRF while at the PASB. 7 Appellants emphasize
the fact that TRF paid Dr. Soper’s salary and benefits in 1947 after he became the Director
of the PASB. However, the payment of wages alone is insufficient to establish an agency
relationship. Standard Oil, 212 U.S. at 225 (stating that, though payment of wages is a
factor to be considered, it is not one of the “ultimate facts” and is only “more or less useful
in determining” which employer’s work is being done and which employer exercised “the
power of control”). Here, there is no indication that TRF was directing or controlling Dr.
Soper’s work at the PASB. In fact, the evidence demonstrates that TRF agreed to pay Dr.
Soper’s salary because the PASB was experiencing financial difficulties. Once the PASB
raised enough money to fund the director position, it began paying Dr. Soper directly.
Appellants further argue that Dr. Soper was doing the work of TRF while at the
PASB because he was furthering TRF’s goal of finding a cure for syphilis. Appellants state
that, because Dr. Soper remained an officer of TRF during 1947, he was not truly on leave
from TRF. This argument is unconvincing. Though Dr. Soper remained an officer of TRF,
he did not communicate with TRF on a regular basis, nor is there evidence that he took
7
In their brief, Appellants cite to multiple items of evidence that were not in the
record considered by the district court. See Carlson v. Bos. Sci. Corp., 856 F.3d 320, 324
(4th Cir. 2017) (“The Federal Rules of Civil Procedure require parties to cite all evidence
in support of their positions at summary judgment, thus permitting a district court to limit
its review to such cited materials.” (citing FED. R. CIV. P. 56(c)(1), (3))). Accordingly, the
Court will not consider evidence cited by Appellants that was not properly before the
district court.
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direction from TRF while Director of the PASB. 8 Dr. Soper stated himself that he “was no
longer with the Foundation.” J.A. 1009. The connection between TRF’s interest in finding
a cure for syphilis and the work that Dr. Soper did while at the PASB is simply far too
attenuated to establish an agency relationship.
Finally, there is insufficient evidence to support Appellants’ argument that Dr.
Soper was a dual agent of TRF and the PASB because, though TRF did not exercise control
over him, it maintained the ability to do so. As previously stated, there is no indication that
TRF had the ability to exercise control over Dr. Soper while at the PASB. Though TRF
paid his salary, Dr. Soper appeared at all times to be doing the work of the PASB. Finally,
the PASB’s constitution, the general terms of which were adopted by the PASB in January
1947, prohibited Dr. Soper from taking outside direction.
The Court sympathizes with the victims of the Guatemala Experiments who suffered
inhumane and unacceptable treatment at the hands of Dr. Soper and others. However,
TRF’s connection to the Experiments is too tenuous to be held liable for them. Because the
Court finds that Dr. Soper was not an agent of TRF, it need not reach TRF’s alternative
arguments.
For the foregoing reasons, we hereby affirm the district court’s grant of summary
judgment in favor of TRF.
AFFIRMED
8
During oral argument, Appellants emphasized the fact that Dr. Soper was required
to send monthly reports to TRF while at the PASB. However, because these reports were
not properly raised before the district court, this Court will not consider them.
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WILKINSON, Circuit Judge, concurring:
The U.S. Army had its first glimpse into the Nazi regime’s horrors when it liberated
the Ohrdruf concentration camp on April 4, 1945. See U.S. Holocaust Memorial Museum,
The 89th Infantry Division During World War II (last accessed Jan. 9, 2024). The scale of
the inhumanity evident in the liberating soldiers’ reports compelled General Eisenhower to
visit. See id. As he walked through the captured Nazi camp, flanked by Generals Bradley
and Patton, Eisenhower witnessed charred human remains strewn across a burning pyre
and the bodies of emaciated victims killed by starvation piled high in a wooden shed. See
id. Eisenhower made it plain that the whole world needed to understand the “brutality and
ruthless disregard of every shred of decency” displayed by the Nazis at Ohrdruf. DWIGHT
D. EISENHOWER, CRUSADE IN EUROPE 408–09 (1948). He immediately requested that the
United States and United Kingdom send journalists and legislators to the camp so there
would be “no room for cynical doubt” as to its horrors. Id. at 409; see also U.S. Holocaust
Memorial Museum, Eisenhower Asks Congress and Press to Witness Nazi Horrors (last
accessed Jan. 9, 2024).
Ohrdruf was just the tip of the iceberg in Nazi Germany’s eugenic campaign to
exterminate the Jewish people and other individuals the campaign’s malignant architects
classified as inferior. When the U.S. Army liberated larger concentration camps like
Buchenwald and Dachau, it confronted even more shocking atrocities. Among the horrors
was evidence of large-scale human experimentation conducted without, to put it mildly,
any consent. At Dachau alone, Nazi scientists intentionally infected prisoners with malaria,
forced other prisoners into a low-pressure chamber to watch them die of simulated altitude
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sickness, and froze yet others alive to study hypothermia. See Peter Tyson, Holocaust on
Trial: The Experiments, PBS NOVA ONLINE (Oct. 2000); U.S. Holocaust Memorial
Museum, Dachau (last accessed Jan. 9, 2024). The camps liberated by the Soviet Army
contained equal horrors, including arbitrary amputations at Ravensbrück and Josef
Mengele’s unconscionable experiments on twin children and other victims at Auschwitz.
See Peter Tyson, Holocaust on Trial: The Experiments, PBS NOVA ONLINE (Oct. 2000).
These revelations helped cast a long shadow over the eugenics movement and
nonconsensual medical experimentation in the United States. The movement was a product
of lingering social Darwinism, which held that the end of survival of the fittest justified an
assortment of dubious means. Yet it is in the means that rights are often most assiduously
safeguarded, an idea which escaped many prominent figures in the early twentieth century
who gravitated toward the errant belief that the end of “improvement” excused sterilizing
assertedly disabled, mentally ill, and marginalized individuals without their consent. See,
e.g., Buck v. Bell, 274 U.S. 200, 205–08 (1927) (Holmes, J.) (upholding a Virginia law that
allowed for the nonconsensual sterilization of “feeble-minded” adults and remarking that
“three generations of imbeciles are enough”).
It is certainly true that America’s eugenics movement was in no sense akin to the
unique atrocities perpetrated by the Nazi regime. It is further true that medical science
requires experimentation to advance, and that experimental treatments and vaccinations,
when undertaken with the full knowledge and consent of their subjects, have brought
incalculable benefits to millions across the globe. But the methods of experimentation are
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all important, and the moral wrongs of regarding “undesirables” as “expendables” sit on
our shoulders still.
Our nation’s confrontation with the horrors of the Holocaust should have awakened
the government to the immense dangers of nonconsensual medical experimentation
conducted in the name of societal progress. Yet the record in this case reveals that, almost
as soon as victory in Europe was achieved, the U.S. Public Health Service directed, funded,
staffed, and executed nonconsensual medical experiments in Guatemala. These
experiments involved, among other horrors, intentionally injecting and exposing over one
thousand nonconsenting children and adults to gonorrhea, syphilis, and other venereal
diseases.
The 1947 Doctors’ Trial at Nuremburg occurred in parallel with the Guatemala
experiments, further sounding the alarm on the impropriety of intentional and
nonconsensual infection of human subjects. See United States v. Stanley, 483 U.S. 669,
687 (1987) (Brennan, J., concurring in part and dissenting in part) (“The medical trials at
Nuremberg in 1947 deeply impressed upon the world that experimentation with unknowing
human subjects is morally and legally unacceptable.”). But the nonconsensual
experimentation continued. Indeed, the Guatemala experiments constitute but one project
in a series of unethical human experimentation by the U.S. government in the mid-
twentieth century. See, e.g., Ctr. for Disease Control, The U.S. Public Health Service
Untreated Syphilis Study at Tuskegee (Jan. 9, 2023); Presidential Commission for the Study
of Bioethical Issues, Ethically Impossible: STD Research in Guatemala from 1946 to 1948,
13–24 (Sept. 2011) (discussing how the Guatemala experiments were presaged by the Terre
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Haute, Indiana experiments, which involved the intentional infection of federal prisoners
with gonorrhea); S. REP. NO. 94-755, at 385–423 (1976) (detailing nonconsensual drug
testing by the CIA and military intelligence on unwitting human subjects in the United
States); Alf S. Alving et al., Procedures Used at Stateville Penitentiary for the Testing of
Potential Antimalarial Agents, 27(3) J. CLINICAL INVESTIGATION 2, 2–5 (May 1, 1948).
Occurring both inside and outside our borders, these experiments primarily targeted
marginalized people who had limited ability to wield political power in their own defense.
See Mike Stobbe, Ugly past of U.S. human experiments uncovered, NBC NEWS (Feb. 27,
2011) (discussing over 40 unethical medical studies conducted by U.S. government
doctors, primarily during the 1940s to 1960s, and observing that “[m]any prominent
researchers felt it was legitimate to experiment on people who did not have full rights in
society”).
These incongruous thoughts of American exposure to the world of the full depravity
of the Holocaust and American participation in the experimentation in Guatemala and
elsewhere reveal the most and least admirable features of our wonderful country. There is
a temptation in cases involving grievous harms such as these to cast the net of liability wide
so as to maximally deter perpetrators and compensate victims. But the record here simply
cannot support an extension of liability to the Rockefeller Foundation. While the
Foundation did employ the Guatemala experiments’ primary investigator, Frederick Soper,
it exercised neither control nor direction over his involvement in the experiments while he
was detailed to lead the intergovernmental Pan American Sanitary Bureau. And the
plaintiffs presented no evidence showing that the Foundation was consulted on the
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Guatemala experiments or apprised of their unethical methods. Alas, it was our own
government, not the Rockefeller Foundation, that was the driving force behind these
monstrous wrongs.
Therefore, as the lead opinion has carefully set forth, the relationship between Soper
and the Rockefeller Foundation is too attenuated to regard him as its agent, rather than as
an agent of the Pan American Sanitary Bureau, with respect to the Guatemala experiments.
I thus concur in that opinion with some sadness, but with a conviction that the rule of law
is not advanced as an instrument of justice by affixing liability where it does not belong.
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