Evidence map›Paper›PMID 30496712›Full record

ArticleJournal of applied physiology (Bethesda, Md. : 1985)2019

B cell homeostasis is maintained during long-duration spaceflight.

Guillaume Spielmann, Nadia Agha, Hawley Kunz, Richard J Simpson, Brian Crucian, Satish Mehta, Mitzi Laughlin, John Campbell

Open access · bronzeAbstract read
In one paragraph

Article in Journal of applied physiology (Bethesda, Md. : 1985), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 13% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 51 citations in OpenAlex.

  1. Pooled it
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  13. Microgravity and immune cells.Journal of the Royal Society, Interface · 2023
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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

8 authors at 6 institutions in 2 countries.

Guillaume SpielmannSchool of Kinesiology, Louisiana State University , Baton Rouge, Louisiana.
Nadia AghaLaboratory of Integrated Physiology, Department of Health and Human Performance, University of Houston , Houston, Texas.
Hawley KunzLaboratory of Integrated Physiology, Department of Health and Human Performance, University of Houston , Houston, Texas.
Richard J SimpsonLaboratory of Integrated Physiology, Department of Health and Human Performance, University of Houston , Houston, Texas.
Brian CrucianNational Aeronautics and Space Administration-Johnson Space Center , Houston, Texas.
Satish MehtaNational Aeronautics and Space Administration-Johnson Space Center , Houston, Texas.
Mitzi LaughlinLaboratory of Integrated Physiology, Department of Health and Human Performance, University of Houston , Houston, Texas.
John CampbellSchool of Kinesiology, Louisiana State University , Baton Rouge, Louisiana.
Louisiana State University · USUniversity of Houston · USJohnson Space Center · USMayo Clinic · USNational Aeronautics and Space Administration · USTexas Orthopedic Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Long-duration spaceflights reportedly induce immune dysregulation, which is considered a risk to astronaut safety and mission success. Recent studies have examined the impact of spaceflight on markers of adaptive and innate immunity, but no study, to date, has comprehensively evaluated humoral immunity and serological markers of B cell function. The aim of this study was to characterize changes in B cell numbers and phenotypes, along with plasma Igs and polyclonal free light chains (FLCs)-near-"real-time" biomarkers of Ig synthesis-in response to an ~6-mo mission to the International Space Station (ISS). Whole-blood samples were collected before flight, during flight ("Early flight," "Mid-flight," and "Late flight"), immediately upon return, and during a recovery period (R + 18, R + 30/R + 33, and R + 60/R + 66) from 23 ISS crew members. B Cell counts and phenotypes were measured throughout the duration of the mission, along with total plasma Ig and FLC levels. There was no effect of spaceflight on the number and proportion of the different B cell subsets. There was no difference in kappa FLC between preflight samples and either in-flight or recovery samples ( P > 0.05), and only a marginal reduction was observed in lambda FLC levels upon return to Earth ( P < 0.05). Furthermore, IgG and IgM remained unchanged during and after spaceflight compared with preflight values ( P > 0.05). Of note, plasma IgA concentrations were elevated in-flight compared with baseline and recovery values ( P < 0.05). These results indicate that B cell homeostasis is maintained during long-duration spaceflight, advocating for potential in-flight vaccination as viable countermeasures against viral reactivation during exploration-class missions.

Indexed as

AstronautsImmunity, HumoralSpace FlightAdultBiomarkersB-Lymphocyte SubsetsFemaleHomeostasisHumansImmunoglobulin AImmunoglobulin GImmunoglobulin kappa-ChainsImmunoglobulin lambda-ChainsImmunoglobulin MImmunoglobulinsMaleBiomarkersImmunoglobulin AImmunoglobulin GImmunoglobulin kappa-ChainsImmunoglobulin lambda-ChainsImmunoglobulin MImmunoglobulinsB cell homeostasisfree light chainsimmunoglobulinslong-duration spaceflight

Identifiers

PMID30496712
PMCPMC6397409
OpenAlexW2903357802

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.