Age, Inflammation, and Disease Location Are Critical Determinants of Intestinal Expression of SARS-CoV-2 Receptor ACE2 and TMPRSS2 in Inflammatory Bowel Disease.

Although the respiratory tract is implicated as the primary portal of entry of the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), gastrointestinal involvement is well-reported, associated with nausea, vomiting, diarrhea, and highly persistent viral particle shedding in feces. ,

There is critical need to establish factors determining susceptibility to Coronavirus Disease 2019 (COVID-19) in patients with inflammatory bowel disease (IBD). Age, comorbidity, disease activity, and exposure to immuno-modulatory and biological therapies provide the basis for new guidelines for risk stratification and shielding.

We hypothesize that expression levels of the SARS-CoV-2 spike protein receptor, angiotensin-converting enzyme 2 (ACE2), may also determine susceptibility to SARS-CoV-2-inflicted damage. Transmembrane serine protease 2 (TMPRSS2) primes the viral spike protein, allowing for the potent binding of ACE2. Both are known to be highly expressed in healthy ileal epithelium, with lower levels in epithelial cells in the colon. We report dysregulated mucosal ACE2 and TMPRSS2 expression in the colon and ileum in IBD, and identify the critical determinants of altered expression.

Methods

We compared RNA expression of ACE2 and TMPRSS2 in blood (paired-end sequencing), ileal, and colonic mucosal biopsies (microarray) from 138 patients with treatment-naïve IBD (cases) and 154 controls, predominantly with functional gastrointestinal disorders (Supplementary Table 1). They were recruited at 6 European centers, between 2012 and 2015, as part of the IBD-Character program (EU Character reference no. 305676). Demographics and further details are given in the supplementary information.

Supplementary Table 1

Group Characteristics

	CD	UC	Controls
n	64	74	154
Age, y	30.2 ± 15.9	38.6 ± 15.5	33.6 ± 14.4
Sex, % female, % (n)	46.9 (30)	40.5 (30)	55.8 (86)
Smoker, % (n)	19.0 (12)	5.4 (4)	19.7 (30)
CRP, mg/L	22.7±36.9	33.6±58.7	4.82±12.5
Characteristics, % (n)	L1 25.0 (16)L2 31.2 (20)L3 43.7 (28)L4 21.8 (14)A1 25.0 (16)A2 50.0 (32)A3 25.0 (16)B1 82.8 (53)B2 9.4 (6)B3 4.7 (3)P 7.8 (5)	E1 25.7 (19)E2 29.7 (22)E3 44.6 (33)
Endoscopic assessment	Mayo subscore 4.74 ± 2.90	Froslie score 6.73 ± 4.78

Results

ACE2 expression in the terminal ileum in controls was 25-fold higher than in the colon (P = 7.0 × 10–14; Supplementary Table 2), consistent with previous reports.

Supplementary Table 2

Expression of ACE2 and TMPRSS2 in the Intestinal Mucosa of Patients With CD, UC, and Controls

		IBD	CD	UC	Controls
Colon	All	163	74	89	191
	ACE2	10.35 ± 0.66∗∗∗	10.17 ± 0.63∗	10.50 ± 0.64∗∗∗	9.94 ± 0.72
	TMPRSS2	12.75 ± 0.56	12.72 ± 0.54	12.77 ± 0.58	12.69 ± 0.51
	Noninflamed	78	47	31
	ACE2	10.10 ± 0.62	10.07 ± 0.64	10.12 ± 0.58
	TMPRSS2	12.67 ± 0.50	12.67 ± 0.51	12.64 ± 0.50
	Inflamed	85	27	58
	ACE2	10.58 ± 0.61∗∗∗,†††	10.32 ± 0.58∗∗	10.69 ± 0.59∗∗∗,†††
	TMPRSS2	12.82 ± 0.60∗,†	12.80 ± 0.59	12.83 ± 0.61∗
T. ileum	All	29	17	12	15
	ACE2	13.84 ± 1.86∗	13.24 ± 2.24	14.68 ± 0.35	14.61 ± 1.43
	TMPRSS2	11.21 ± 0.75∗	11.18 ± 0.87	11.25 ± 0.57	10.89 ± 0.55
	Noninflamed	17	6	11
	ACE2	14.12 ± 1.59	13.05 ± 2.38	14.70 ± 0.36
	TMPRSS2	11.42 ± 0.70∗∗	11.69 ± 0.87∗	11.27 ± 0.59∗
	Inflamed	12	11	1
	ACE2	13.44 ± 2.19∗	13.34 ± 2.27∗	14.51
	TMPRSS2	10.91 ± 0.74	10.91 ± 0.78	11.03

NOTE. CD and UC data are compared with controls with ∗ denoting P < .05, ∗∗ < .01, ∗∗∗ < .001. Inflamed and noninflamed tissue is compared within subgroups defined by group and location with † denoting P < .05, †† < .01, ††† < .001. Values significantly different from control are printed in bold. Expression is represented as log2(16+intensity). The Mann-Whitney U test was used.

In IBD, expression in the terminal ileum was increased 10-fold compared with the colon (P = 7.9 × 10–14). In contrast, TMPRSS2 expression in the terminal ileum was lower than in the colon, both in controls (P = 3.6 × 10–16), and in IBD overall (P = 6.0 × 10–19).

Dysregulated Ileal Gene Expression

The expression of ACE2 in inflamed Crohn’s disease (CD) ileum was 60% lower (P = .0175) than in controls (Figure 1 A). Ileal TMPRSS2 was higher in CD noninflamed tissue than in controls (by 70%, P = .023, Figure 1 B). Ileal ACE2 did not differ between patients with ulcerative colitis (UC) and controls, but ileal TMPRSS2 was 30% higher (P = .023, Figure 1 B).

Figure 1

ACE2 and TMPRSS2 expression in ulcerative colitis (UC) and Crohn's disease (CD); shown as log2(16+intensity). OSM – oncostatin M.

Dysregulated Colonic Expression

In CD, colonic ACE2 expression was increased by 30% relative to control (P = .006; Figure 1 C). TMPRSS2 expression in CD colon was similar to controls (Figure 1 D). In UC, the inflamed colonic mucosa expressed 70% more (P = 2.1 × 10–11) ACE2 transcript copies. UC mucosal ACE2 was 50% higher in inflamed vs noninflamed sites (P = 6.3 × 10–5).

Univariate Analyses of Factors Influencing Gene Expression

Colonic ACE2 levels associated with Montreal disease extent (Figure 1 E) and the Mayo endoscopic subscore (rho = 0.43, P = 3.2 × 10–5, Figure 1 F). Colonic TMPRSS2 was upregulated by inflammation (P = .0179, Figure 1 D), and extent (E1 vs E3: 150%, P = .0002, Figure 1 G), and was greater by 20% in men (P = .03).

Among patients with IBD, colonic ACE2 expression correlated weakly with high-sensitivity C-reactive protein (hsCRP) (rho = 0.23, P = .0043), age (rho = 0.19, P = .014, Figure 1 H) and serum albumin (rho = −0.17, P = .037). In controls, colonic ACE2 expression correlated with fecal calprotectin (n = 136, rho = 0.39, P = 2.7 × 10–6), hsCRP (n = 180, rho = 0.25, P = .00083), and age (rho = 0.20, P = .0066). In the control ileum tissue, ACE2 increased with age (rho = 0.64, P = .0099) and was 130% greater in men (P = .0256). The colonic expression of TMPRSS2, but not ACE2, was 20% higher in smokers from the control group (P = .0034). We found no important differences in ACE2 and TMPRSS2 expression with regard to recruitment centers.

We examined the relationship between mucosal ACE2 or TMPRSS2 and blood expression of TNF, OSM, IL10, TGFB1, GATA3, and STAT6 in IBD. Colonic (and also ileal) ACE2 correlated with blood OSM in patients with UC (rho = 0.35, P = .00076, Figure 1 I).

Dysregulation of the Renin-Angiotensin System

Mucosal angiotensinogen correlated with tissue inflammation (P = 4.7 × 10–11 in UC colon, P = 2.0 × 10–5 in CD colon) and disease severity (Mayo subscore rho = 0.58, P = 5.3 × 10–22; Froslie score rho = 0.39, P = 3.4 × 10–9). ACE expression in the blood associated negatively with IBD status (in UC P = 2.4 × 10–6, in CD P = 8.2 × 10–5) but ACE expression was greater in inflamed UC colon (P = .019). Renin was detectable in biopsies only, where it was reduced in colonic IBD compared with controls (UC P = 1.4 × 10–5, CD P = .0034).

Multivariable Analyses

Colonic expression

Multivariable analysis of ACE2 and TMPRSS2 expression were performed (Supplementary Methods). ACE2 gene expression in the colon was associated with increasing age in controls (β = 0.17, 95% confidence interval [CI] 0.02–0.32); with inflammation at biopsy site (β = 0.30, 95% CI 0.10–0.49) and E3 extent in UC (β = 0.40, 95% CI 0.18–0.62) and with endoscopic inflammatory subscore in CD (β = 0.23, 95% CI 0.00–0.46). Colonic TMPRSS2 expression was associated with hsCRP (β = 0.22, 95% CI 0.07–0.37) and smoking status in controls (β = 0.17, 95% CI 0.02–0.32), with Mayo subscore in UC (β = 0.23, 95% CI 0.01–0.44) and none of the parameters in IBD and CD.

Ileal expression

On multivariable analysis, ACE2 gene expression in the ileum was lower in the few patients with CD with B2 or B3 disease (β = −1.09, 95% CI −1.57 to −0.61). No other factors were implicated.

Discussion

We demonstrate that age, the presence of inflammation, and anatomic location are key determinants of expression of ACE2 and TMPRSS2 in patients presenting with IBD. These findings have potential implications for disease management, as well for mechanistic studies. Thus, the inflammation-related increase in ACE2 expression in the colon is consistent with recent mechanistic data highlighting the influence of cytokines on ACE2 expression in the respiratory epithelium. These data raise the possibility that active IBD may enhance viral particle production and uptake in the colon; and, furthermore, that infection and consequent inflammatory activation may exacerbate colitis.

The apparent reduction in ACE2 in the ileum in active CD also bears further investigation: this alteration may relate to the loss of epithelial surface in active ulceration, reduced ACE2 production by maturating epithelium, and consequent sampling effects; or may indeed be directly relevant to CD pathogenesis.

In summary, we identify age, smoking, and active disease as potential additional risk factors of vulnerability to COVID-19 in patients with IBD, through alterations of receptor expression. Our findings lend support to registry initiatives such as SECURE-IBD, which are necessary to monitor the possible impact of COVID-19 on IBD, and to the ongoing translational research program characterizing sites for therapeutic intervention in the molecular pathways of SARS-CoV-2 recognition.