2021
DOI: 10.1111/bjd.19461
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Exploring the human hair follicle microbiome*

Abstract: The writing of this review was made possible through the Monasterium Laboratory, Germany, and startup funds to R.P. from the University of Miami. T.L. acknowledges funding by the DFG CRC 1182 (TPC4.2). T.C.G.B. gratefully appreciates support of the Canadian Institute for Advanced Research (CIFAR) and the DFG CRC 1182.

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Cited by 75 publications
(90 citation statements)
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References 197 publications
(310 reference statements)
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“…Both Porphyromonas and Prevotella are most prevalent organisms on mucosal surfaces, including in the oral cavity, colon and tongue [42]. Porphyromonas and Prevotella in the skin microbiome may contribute to the pathogenesis of HS through upregulation of antimicrobial peptide (AMP) secretion, which in turn increases keratinocyte proliferation and recruitment of macrophages and neutrophils [43]. Porphyromonas gingivalis is an oral periodontopathogen and is implicated in the pathogenesis of periodontitis.…”
Section: Relevance Of the Findingsmentioning
confidence: 99%
“…Both Porphyromonas and Prevotella are most prevalent organisms on mucosal surfaces, including in the oral cavity, colon and tongue [42]. Porphyromonas and Prevotella in the skin microbiome may contribute to the pathogenesis of HS through upregulation of antimicrobial peptide (AMP) secretion, which in turn increases keratinocyte proliferation and recruitment of macrophages and neutrophils [43]. Porphyromonas gingivalis is an oral periodontopathogen and is implicated in the pathogenesis of periodontitis.…”
Section: Relevance Of the Findingsmentioning
confidence: 99%
“…A more decidedly microbiological focus in AA research is further supported by the potential therapeutic effect of fecal microbiota transplants (Rebello et al, 2017) and the currently discussed role of intestinal dysbiosis in AA (Borde and Å strand, 2018). Recent murine studies on the key role commensal microbes and the HF-derived chemokine production controlled by them in the recruitment of regulatory T cells into neonatal skin (Scharschmidt et al, 2017) and the demonstration that HF keratinocyte-derived cytokines maintain skin-resident innate lymphocyte subpopulations which subsequently modulate the skin microbiome by regulating sebocyte functions and sebum production (Kobayashi et al, 2019) encourage one only further to explore the as yet unknown role of the HF microbiome and its dysbiosis in human AA pathobiology (Polak-Witka et al, 2019;Lousada et al, 2020).…”
Section: Beyond the Cd8d T Cell Horizonmentioning
confidence: 99%
“…While it is accepted that the microbiome is a key modulator of host physiology, S1 it remains unknown whether the hair follicle (HF) microbiome affects human hair growth. 1,2 Both traditionally microbial-associated HF diseases, namely acne vulgaris and hidradenitis suppurativa, and hair loss diseases, such as alopecia areata, androgenic alopecia (AGA) and scarring alopecias, are associated with microbiome imbalance S2-S7 , and many are routinely treated with antibiotics. 2,S8 Therefore, it is clinically and biologically relevant to assess if these drugs impact human hair growth, through a microbiota-dependent mechanism.…”
mentioning
confidence: 99%
“…Several antibiotics are associated with hair growth alterations. 2 For example, roxithromycin (RXM) promotes hair growth and antagonizes catagen in patients with AGA, presumably by inhibiting keratinocyte apoptosis. 3 While these hair effects could also derive from macrolide-iduced immunomodulations, S9 interestingly, in AGA the HF microbiome shows dysbiosis, characterized by an increased abundance of (RXM-susceptible) Cutibacterium acnes.…”
mentioning
confidence: 99%