# Elevated Serum Lipopolysaccharides and Intrinsic Factor Autoantibodies Correlate With Macrocytic Anemia Among People With HIV

**Authors:** Daniel Amakye, Samuel Hammond, Osbourne Quaye, Upal Roy, Peter Puplampu, Vincent Ganu, Emmanuel Ayitey Tagoe

PMC · DOI: 10.1002/iid3.70378 · Immunity, Inflammation and Disease · 2026-02-22

## TL;DR

People with HIV are more likely to have macrocytic anemia, which is linked to gut microbial translocation and autoantibodies.

## Contribution

This study is the first to report elevated LPS and intrinsic factor autoantibodies in HIV patients with macrocytic anemia.

## Key findings

- PWH had a 43.6% prevalence of macrocytic anemia compared to 1.8% in HIV-negative individuals.
- Elevated LPS and intrinsic factor autoantibodies correlated strongly with increased mean corpuscular volume in PWH.

## Abstract

Human immunodeficiency virus (HIV) infection is associated with various comorbidities, including macrocytic anemia, though the role of the infection is unclear. HIV has been implicated in microbial translocation and altered immune responses. This study aimed to establish the relationship between gut microbial translocation and immune response, and macrocytic anemia among people with HIV (PWH).

Fifty‐five PWH on combination antiretroviral therapy (cART) were age‐matched with 55 HIV‐negative individuals. Demographic data and blood samples were collected from February to July 2023. Hematological indices, including red blood cell (RBC) count, hemoglobin concentration, and mean corpuscular volume (MCV), were measured. Serum lipopolysaccharides (LPS) and intrinsic factor autoantibodies (IFAA) were measured using ELISA.

The prevalence of macrocytic anemia was significantly higher in the HIV cohort (43.6%) compared to HIV‐negative individuals (1.8%), (p < 0.0001). PWH exhibited higher microbial translocation, characterized by elevated LPS levels (p < 0.0001). PWH with macrocytic anemia showed significantly increased serum LPS and IFAA levels compared to those without anemia (p < 0.001). Intrinsic factor autoantibodies correlated positively with systolic (r = 0.49, p < 0.001) and diastolic blood pressures (r = 0.31, p < 0.01), as well as LPS (r = 0.60, p < 0.001) and MCV (r = 0.65, p < 0.001).

This study reports for the first time elevated lipopolysaccharides and intrinsic factor autoantibodies among PWH, and the lipopolysaccharides and intrinsic factor autoantibodies strongly correlated with mean corpuscular volume in the patients. Targeting serum lipopolysaccharides and intrinsic factor autoantibodies may offer a novel therapeutic strategy.

## Linked entities

- **Diseases:** macrocytic anemia (MONDO:0002281)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, HAMP (hepcidin antimicrobial peptide) [NCBI Gene 57817] {aka HEPC, HFE2B, LEAP1, PLTR}
- **Diseases:** hematological abnormality (MESH:D006402), hypertension (MESH:D006973), nutritional deficiencies (MESH:D044342), stomach ulcers (MESH:D013276), Anemia (MESH:D000740), chronic inflammation (MESH:D007249), liver disease (MESH:D008107), Co-morbidities (MESH:D060085), neurological complications (MESH:D002493), insulin resistance (MESH:D007333), immune (MESH:D007154), bone marrow suppression (MESH:D001855), sarcoidosis (MESH:D012507), GBS (MESH:D020275), Cancer (MESH:D009369), cardiovascular disease (MESH:D002318), encephalitis (MESH:D004660), Microcytosis (OMIM:616959), infection (MESH:D007239), systemic (MESH:D015619), Vitamin B12 deficiency (MESH:D014806), IM (MESH:D009220), damage of the gastrointestinal tract (MESH:D005770), hepatitis (MESH:D056486), Macrocytosis (MESH:C564004), Autoimmune disorders (MESH:D001327), immune thrombocytopenic purpura (MESH:D016553), leaky gut syndrome (MESH:C535298), Macrocytic Anemia (MESH:D000748), AIDS (MESH:D000163), anemia of chronic disease (MESH:D002908), myasthenia gravis (MESH:D009157), Infectious (MESH:D003141), nutritional deficit (MESH:D009748), Graves' disease (MESH:D006111), autoimmune hepatitis (MESH:D019693), pernicious anemia (MESH:D000752), immune dysregulation (OMIM:614878), HIV (MESH:D015658)
- **Chemicals:** oxygen (MESH:D010100), Zidovudine (MESH:D015215), B-complex (-), Abacavir (MESH:C106538), MMA (MESH:D008764), EDTA (MESH:D004492), Vitamin B12 (MESH:D014805), dolutegravir (MESH:C562325), LPS (MESH:D008070), Stavudine (MESH:D018119), iron (MESH:D007501), efavirenz (MESH:C098320), darunavir (MESH:D000069454), B12 (MESH:C034730), folate (MESH:D005492), alcohol (MESH:D000438)
- **Species:** Human immunodeficiency virus (species) [taxon 12721], Homo sapiens (human, species) [taxon 9606], Human immunodeficiency virus 1 (no rank) [taxon 11676], Sus scrofa (pig, species) [taxon 9823]
- **Mutations:** C665T

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12928062/full.md

## References

38 references — full list in the complete paper: https://tomesphere.com/paper/PMC12928062/full.md

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Source: https://tomesphere.com/paper/PMC12928062