Evidence map›Paper›PMID 33224136›Full record

ArticleFrontiers in immunology2020

Neutrophil-to-Lymphocyte Ratio: A Biomarker to Monitor the Immune Status of Astronauts.

Amber M Paul, Siddhita D Mhatre, Egle Cekanaviciute, Ann-Sofie Schreurs, Candice G T Tahimic, Ruth K Globus, Sulekha Anand, Brian E Crucian, Sharmila Bhattacharya

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

38 citing papers in PubMed, 68 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Telomeres in Space.Aging cell · 2025
    Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Antidepressant-like Effects ofPharmaceuticals (Basel, Switzerland) · 2024
    Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. Review
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

9 authors at 6 institutions in 1 country.

Amber M PaulSpace Biosciences Division, NASA Ames Research Center, Moffett Field, CA, United States.
Siddhita D MhatreSpace Biosciences Division, NASA Ames Research Center, Moffett Field, CA, United States.
Egle CekanaviciuteSpace Biosciences Division, NASA Ames Research Center, Moffett Field, CA, United States.
Ann-Sofie SchreursSpace Biosciences Division, NASA Ames Research Center, Moffett Field, CA, United States.
Candice G T TahimicSpace Biosciences Division, NASA Ames Research Center, Moffett Field, CA, United States.
Ruth K GlobusSpace Biosciences Division, NASA Ames Research Center, Moffett Field, CA, United States.
Sulekha AnandDepartment of Biological Sciences, San Jose State University, San Jose, CA, United States.
Brian E CrucianBiomedical Research and Environmental Sciences Division, NASA Johnson Science Center, Houston, TX, United States.
Sharmila BhattacharyaSpace Biosciences Division, NASA Ames Research Center, Moffett Field, CA, United States.
Ames Research Center · USJohnson Space Center · USKBR (United States) · USSan Jose State University · USUniversities Space Research Association · USUniversity of North Florida · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A comprehensive understanding of spaceflight factors involved in immune dysfunction and the evaluation of biomarkers to assess in-flight astronaut health are essential goals for NASA. An elevated neutrophil-to-lymphocyte ratio (NLR) is a potential biomarker candidate, as leukocyte differentials are altered during spaceflight. In the reduced gravity environment of space, rodents and astronauts displayed elevated NLR and granulocyte-to-lymphocyte ratios (GLR), respectively. To simulate microgravity using two well-established ground-based models, we cultured human whole blood-leukocytes in high-aspect rotating wall vessels (HARV-RWV) and used hindlimb unloaded (HU) mice. Both HARV-RWV simulation of leukocytes and HU-exposed mice showed elevated NLR profiles comparable to spaceflight exposed samples. To assess mechanisms involved, we found the simulated microgravity HARV-RWV model resulted in an imbalance of redox processes and activation of myeloperoxidase-producing inflammatory neutrophils, while antioxidant treatment reversed these effects. In the simulated microgravity HU model, mitochondrial catalase-transgenic mice that have reduced oxidative stress responses showed reduced neutrophil counts, NLR, and a dampened release of selective inflammatory cytokines compared to wildtype HU mice, suggesting simulated microgravity induced oxidative stress responses that triggered inflammation. In brief, both spaceflight and simulated microgravity models caused elevated NLR, indicating this as a potential biomarker for future in-flight immune health monitoring.

Indexed as

AstronautsHealth StatusAnimalsBiomarkersBlood DonorsCells, CulturedCytokinesFemaleGranulocytesHumansInflammationLymphocytesMaleMiceMice, Inbred C57BLMice, TransgenicBiomarkersCytokinesinflammationneutrophilsNLRoxidative stress responsesimulated microgravityspaceflight

Identifiers

PMID33224136
PMCPMC7667275
OpenAlexW3094637207

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.