Evidence map›Paper›PMID 29261698›Full record

ArticlePloS one2017

Effects of transportation, relocation, and acclimation on phenotypes and functional characteristics of peripheral blood lymphocytes in rhesus monkeys (Macaca mulatta).

Pramod N Nehete, Kathryn A Shelton, Bharti P Nehete, Sriram Chitta, Lawrence E Williams, Steven J Schapiro, Christian R Abee

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 27 citations in OpenAlex.

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  14. Effects of Transportation and Relocation on Immunologic Measures in Cynomolgus Macaques (Journal of the American Association for Laboratory Animal Science : JAALAS · 2019
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 2 countries.

Pramod N NeheteDepartment of Veterinary Sciences, The University of Texas MD Anderson Cancer Center, Bastrop, Texas, United States of America.ORCID http://orcid.org/0000-0002-2815-2677
Kathryn A SheltonDepartment of Veterinary Sciences, The University of Texas MD Anderson Cancer Center, Bastrop, Texas, United States of America.
Bharti P NeheteDepartment of Veterinary Sciences, The University of Texas MD Anderson Cancer Center, Bastrop, Texas, United States of America.
Sriram ChittaDepartment of Veterinary Sciences, The University of Texas MD Anderson Cancer Center, Bastrop, Texas, United States of America.
Lawrence E WilliamsDepartment of Veterinary Sciences, The University of Texas MD Anderson Cancer Center, Bastrop, Texas, United States of America.
Steven J SchapiroDepartment of Veterinary Sciences, The University of Texas MD Anderson Cancer Center, Bastrop, Texas, United States of America.
Christian R AbeeDepartment of Veterinary Sciences, The University of Texas MD Anderson Cancer Center, Bastrop, Texas, United States of America.
The University of Texas MD Anderson Cancer Center · USUniversity of Copenhagen · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Nonhuman primates from domestic sources constitute a small, but critical, proportion of animals studied in research laboratories. Many of these nonhuman primates are raised at one facility and subsequently transported/relocated to another facility for research purposes. We examined the effects of transport, relocation, and acclimation on the phenotype and function of peripheral blood mononuclear cells (PBMCs) in a group of rhesus monkeys that were transported by road for approximately 21 hours from one facility to another. Using a panel of human antibodies and a set of standardized human immune assays, we evaluated the phenotype of lymphocyte subsets by flow, mitogen-specific immune responses of PBMCs in vitro, and levels of circulating cytokines and cortisol in plasma at various time points including immediately before transport, immediately upon arrival, and after approximately 30 days of acclimation. Analyses of blood samples revealed that CD3+ T-cell and CD20+ B-cell populations had decreased significantly immediately after relocation but had recovered within 30 days after arrival at the new facility. Similarly, circulating cortisol and cytokine levels in plasma were significantly higher immediately after relocation; and by the 30-day time point, these differences were no longer significant. However, immune assays of PBMCs indicated that mitogen-specific responses for proliferation, interferon γ (IFN-γ), and perforin were significantly higher after relocation and 30 days of acclimation. These findings have implications on the research participation of transported and relocated nonhuman primates in immunologic research studies, suggesting that 30 days is not sufficient to ensure return to baseline immune homeostasis. These data should be considered when planning research studies in order to minimize potential confounding factors associated with relocation and to maximize study validity.

Indexed as

AcclimatizationTransportationAnimalsBiomarkersCell ProliferationCytokinesEnzyme-Linked Immunospot AssayFemaleHydrocortisoneInterferon-gammaLymphocytesLymphocyte SubsetsMacaca mulattaMaleMitogensPerforinBiomarkersCytokinesHydrocortisoneInterferon-gammaMitogensPerforin

Identifiers

PMID29261698
PMCPMC5736198
OpenAlexW2780851716

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.