# Assessment of IL28 (rs12980275) and (rs8099917) Frequency in Recurrent Ocular Herpes Simplex Virus (HSV) Infection

**Authors:** Borivoje Savic, Bozidar Savic, Tanja Kalezic, Bojana Dacic-Krnjaja, Veljko Milosevic, Sanja Petrovic Pajic, Vesna Maric, Tiana Petrovic, Svetlana Stanojlovic

PMC · DOI: 10.3390/life15030389 · Life · 2025-03-01

## TL;DR

This study found that specific genetic variations in IL28 are linked to a lower risk of recurring eye infections caused by the herpes simplex virus.

## Contribution

The study identifies specific IL28 gene polymorphisms associated with reduced recurrence of ocular herpes simplex virus infections.

## Key findings

- Recurrent HSV keratitis was significantly associated with certain IL28 SNP genotypes (p < 0.01).
- Patients with homozygous GG polymorphism for both SNPs did not develop recurrent HSV keratitis.
- The most common SNPs in recurrent HSV disease were heterozygous AG rs12980275 and GT rs8099917.

## Abstract

(1) Introduction: The main way of spreading the herpes simplex virus 1 (HSV-1) is through direct contact, as the virus enters the host via mucous membranes. Ocular infection can occur as a primary infection or as a recurrent one. The movement of HSV-1 along the ophthalmic branch of the fifth cranial nerve from its latency phase in the trigeminal ganglion and its activation represent a process influenced by various symbiotic factors, such as environmental conditions and the host’s genetic characteristics. The aim of this study was to assess the frequency of IL28 (rs12980275) and (rs8099917) in recurrent ocular HSV infections. (2) Materials and methods: The study included 60 patients aged over 18, of both sexes, all of whom had a history of herpes simplex labialis (HSL). Patients were tested for HSV-1-specific IgG antibodies, and seropositive individuals were genotyped for single nucleotide polymorphisms (SNPs) rs12980275 and rs8099917. A total of 57 seropositive patients were included in the study. (3) Results: A statistically significant association was found between recurrent HSV keratitis (HSK) and heterozygous GT rs8099917 and homozygous TT rs8099917, as well as heterozygous AG rs12980275 and homozygous AA rs12980275 (p < 0.01). Interestingly, patients with homozygous GG polymorphism for both genotypes GG rs8099917 and GG rs12980275 did not develop recurrent HSV keratitis. (4) Conclusion: The most frequent SNP variations in patients with recurrent HSV disease were heterozygous AG rs12980275 (61.40%) and heterozygous GT rs8099917 (52.63%). Patients with recurrent HSV keratitis lacked the homozygous GG polymorphism in both GG rs8099917 and GG rs12980275 genotypes, suggesting that HSV-seropositive individuals expressing these genotypes may have lower predisposition to develop recurrent stromal HSV keratitis.

## Linked entities

- **Genes:** Ifnl3 (interferon lambda 3) [NCBI Gene 338374]
- **Diseases:** HSV keratitis (MONDO:0015288)

## Full-text entities

- **Genes:** IFNL3 (interferon lambda 3) [NCBI Gene 282617] {aka IFN-lambda-3, IFN-lambda-4, IL-28B, IL-28C, IL28B, IL28C}
- **Diseases:** HSV disease (MESH:D006561), Ocular infection (MESH:D015817), HSL (MESH:D006560), infection (MESH:D007239), seropositive (MESH:D006679), HSK (MESH:D016849)
- **Species:** Homo sapiens (human, species) [taxon 9606], Human alphaherpesvirus 1 (Herpes simplex virus type 1, no rank) [taxon 10298]
- **Mutations:** rs12980275, rs8099917

## Full text

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## Figures

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## References

20 references — full list in the complete paper: https://tomesphere.com/paper/PMC11944099/full.md

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Source: https://tomesphere.com/paper/PMC11944099