Evidence map›Paper›PMID 39109956›Full record

ArticleImmunoHorizons2024

Effects of Perfluorohexane Sulfonate Exposure on Immune Cell Populations in Naive Mice.

Timothy M Pierpont, Jessica Elmore, Amie Redko, Orchi Anannya, Brian Imbiakha, Katelyn O'Hare, Alanis Villanueva, Sasha Anronikov, Narda Bondah, Sue Chang and 2 more

Abstract read
In one paragraph

Article in ImmunoHorizons, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Review
  2. Article
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

12 authors.

Timothy M PierpontDepartment of Microbiology & Immunology, Cornell University, Ithaca, NY.
Jessica ElmoreDepartment of Microbiology & Immunology, Cornell University, Ithaca, NY.ORCID 0000-0002-4360-0378
Amie RedkoDepartment of Microbiology & Immunology, Cornell University, Ithaca, NY.
Orchi AnannyaDepartment of Microbiology & Immunology, Cornell University, Ithaca, NY.ORCID 0000-0003-0536-5829
Brian ImbiakhaDepartment of Microbiology & Immunology, Cornell University, Ithaca, NY.
Katelyn O'HareDepartment of Microbiology & Immunology, Cornell University, Ithaca, NY.ORCID 0009-0007-3380-2527
Alanis VillanuevaDepartment of Microbiology & Immunology, Cornell University, Ithaca, NY.ORCID 0000-0003-3608-0148
Sasha AnronikovDepartment of Microbiology & Immunology, Cornell University, Ithaca, NY.ORCID 0000-0001-7854-1809
Narda BondahDepartment of Microbiology & Immunology, Cornell University, Ithaca, NY.ORCID 0000-0001-8474-2252
Sue Chang3M Company, St. Paul, MN.ORCID 0000-0003-4282-7199
Julie SahlerDepartment of Microbiology & Immunology, Cornell University, Ithaca, NY.ORCID 0000-0003-1852-9511
Avery AugustDepartment of Microbiology & Immunology, Cornell University, Ithaca, NY.ORCID 0000-0003-4968-3415

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Perfluorohexane sulfonate (PFHxS) is a member of the per- and polyfluoroalkyls (PFAS) superfamily of molecules, characterized by their fluorinated carbon chains and use in a wide range of industrial applications. PFHxS and perfluorooctane sulfonate are able to accumulate in the environment and in humans with the approximated serum elimination half-life in the range of several years. More recently, some PFAS compounds have also been suggested as potential immunosuppressants. In this study, we analyze immune cell numbers in mice following 28-d repeated oral exposure to potassium PFHxS at 12, 120, 1,200, and 12,000 ng/kg/d, with resulting serum levels ranging up to ∼1,600 ng/ml, approximating ranges found in the general population and at higher levels in PFAS workers. The immunosuppressant cyclophosphamide was analyzed as a positive control. B cells, T cells, and granulocytes from the bone marrow, liver, spleen, lymph nodes, and thymus were evaluated. We found that at these exposures, there was no effect of PFHxS on major T or B cell populations, macrophages, dendritic cells, basophils, mast cells, eosinophils, neutrophils, or circulating Ab isotypes. By contrast, mice exposed to cyclophosphamide exhibited depletion of several granulocyte and T and B cell populations in the thymus, bone marrow, and spleen, as well as reductions in IgG1, IgG2b, IgG2c, IgG3, IgE, and IgM. These data indicate that exposures of up to 12,000 ng/kg of PFHxS for 28 d do not affect immune cell numbers in naive mice, which provides valuable information for assessing the risks and health influences of exposures to this compound.

Indexed as

FluorocarbonsAnimalsB-LymphocytesFemaleGranulocytesMaleMiceSpleenSulfonic AcidsThymus GlandT-LymphocytesFluorocarbonsperfluorohexanesulfonic acidSulfonic Acids

Identifiers

PMID39109956
PMCPMC11374752

What OpenQuestion holds

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Registered trials

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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.