Next Article in Journal
Genomic Characterization of Dengue Virus Outbreak in 2022 from Pakistan
Next Article in Special Issue
Consistency of Bacterial Triggers in the Pathogenesis of Hidradenitis Suppurativa
Previous Article in Journal
Omicron Variant of SARS-CoV-2: An Indian Perspective of Vaccination and Management
Previous Article in Special Issue
Allelic Variants of HLA-C Upstream Region, PSORS1C3, MICA, TNFA and Genes Involved in Epidermal Homeostasis and Barrier Function Influence the Clinical Response to Anti-IL-12/IL-23 Treatment of Patients with Psoriasis
 
 
Brief Report
Peer-Review Record

Autoinflammation in Syndromic Hidradenitis Suppurativa: The Role of AIM2

Vaccines 2023, 11(1), 162; https://doi.org/10.3390/vaccines11010162
by Chiara Moltrasio 1,2,*,†, Rachele Cagliani 3,†, Manuela Sironi 3, Mario Clerici 4,5, Chiara Pontremoli 3, Carlo Alberto Maronese 1,4, Paola Maura Tricarico 6, Sergio Crovella 7 and Angelo Valerio Marzano 1,4
Reviewer 1: Anonymous
Vaccines 2023, 11(1), 162; https://doi.org/10.3390/vaccines11010162
Submission received: 12 December 2022 / Revised: 6 January 2023 / Accepted: 10 January 2023 / Published: 11 January 2023
(This article belongs to the Special Issue Advances in Skin Immune-Mediated Disease)

Round 1

Reviewer 1 Report

It was a pleasure for me to read this interesting paper. The purpose, focusing on inflammasome and its activation pathways, has great scientific relevance at present time and the article is well structured. The weakness of small sample size was already declared by AA. In my opinion the manuscript is already suitable for publication as it is.

Author Response

We would like to thank the Reviewer for the positive comments and the appreciation of our work.

Reviewer 2 Report

Syndromic HS represents a group of syndromes with clinical signs exhibiting an autoinflammatory background as common denominator. The syndromes are rare and include Hs as one of their major signs. While several research groups concentrate their work on the elucidation of HS etiopathogenesis, there is only a few information on the pathology of syndromic HS and especially any common molecular background.

Since autoinflammatory diseases are likely to at least partially be interferonopathies, it is consequent that the authors, experts in the field of syndromic HS, looked for the expression of the human IFN-inducible protein absent in melanoma 2 (AIM2) gene in these diseases.

The data presented are preliminary and a small number of patients have been included in the study, but the data are valuable for the presentation of the concept and as background for further larger studies.

Author Response

We would like to thank the Reviewer for the positive comments and the appreciation of our work.

 

Reviewer 3 Report

Table 1 format: please check the treatment/follow up column. The PDF format I reviewed did not align.

Line 139-line 161: when using parenthesis, make it clear the number is referring to the patient ID in the table. It may be confusing if it may reflect the number of patients with the condition.

line 144. clarify "mean". I suppose the mean score of at first evaluation from these patients.

Line 147: what 30.5 vs 25.9 reflected? The average age at onset of these patients? clarify.

line 163: rs41264459 variant - explain in the introduction. 

Figure 1: improve the visuals. Not clear.

Line 189-191/246-248. It is not clear. Rewrite. It is easier to understand the language in the abstract

.

Author Response

Please see the attachment.

Author Response File: Author Response.docx

Back to TopTop