Rahmoun Massilva, Aussel Audrey, Bouzidi Sarah, Pedergnana Vincent, Malassigné Victor, Puech Julien, Veyer David, Péré Hélène, Lepine Charles, Blanc Fabian, Boulle Nathalie, Costes-Martineau Valérie, Bravo Ignacio G
Laboratory MIVEGEC (Univ Montpellier, CNRS, IRD), French National Center for Scientific Research (CNRS), Montpellier, France.
Service D'anatomie et Cytologie pathologiques, CHU de Montpellier, Montpellier, France.
Tumour Virus Res. 2024 Dec;18:200294. doi: 10.1016/j.tvr.2024.200294. Epub 2024 Oct 29.
Recurrent respiratory papillomatosis (RRP) is a rare, proliferative disease caused by human papillomavirus 6 (HPV6) and HPV11. RRP can occasionally spread and undergo malignant transformation. We analysed samples across time for five RRP patients with malignant transformation and four with highly recurrent, non-malignant RRP by applying high-throughput sequencing. Patients with malignant transformation were infected by HPV11_A1/A2, while most non-malignant cases were associated with HPV6. Transient multiple infections with HPV6 and HPV11 were found in two patients, and resolved later to single infections. Viral genome loads were homogeneous across groups (median = 78 viral genomes per human genome). Within-patient, we did not observe differences between the viral sequences in the papillomatous lesions and in the malignant tissue. Genetic analysis of the NLRP1 gene revealed no known mutations linked to idiopathic RRP, though some novel variants merit to be explored in larger cohorts. HPV11 infections appear associated with RRP malignant transformation in young patients. Multiple infections can occur in RRP, but within-patient viral diversity is minimal for a given genotype. Our results confirm the importance of viral genotype in disease prognosis and are consistent with growing evidence of HPV11 infections to be differentially associated with RRP malignant transformation in young patients.
复发性呼吸道乳头状瘤病(RRP)是一种由人乳头瘤病毒6型(HPV6)和HPV11引起的罕见增殖性疾病。RRP偶尔会扩散并发生恶性转化。我们通过高通量测序分析了5例发生恶性转化的RRP患者和4例高度复发的非恶性RRP患者不同时间的样本。发生恶性转化的患者感染的是HPV11_A1/A2,而大多数非恶性病例与HPV6相关。在两名患者中发现了HPV6和HPV11的短暂多重感染,随后转变为单一感染。各组间病毒基因组负荷相同(中位数为每人类基因组78个病毒基因组)。在患者体内,我们未观察到乳头状瘤病变和恶性组织中病毒序列之间的差异。NLRP1基因的遗传分析未发现与特发性RRP相关的已知突变,不过一些新的变异值得在更大的队列中进行探索。HPV11感染似乎与年轻患者的RRP恶性转化有关。RRP中可发生多重感染,但对于给定的基因型,患者体内的病毒多样性最小。我们的结果证实了病毒基因型在疾病预后中的重要性,并且与越来越多的证据一致,即HPV11感染与年轻患者的RRP恶性转化存在差异关联。