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Clinical features of cryptococcosis in patients with different immune statuses: a multicenter study in Jiangsu Province–China
BMC Infectious Diseases volume 21, Article number: 1043 (2021)
Current guidelines support different management of cryptococcosis between severely immunodeficient and immunocompetent populations. However, few studies have focused on cryptococcosis patients with mild-to-moderate immunodeficiency. We performed this study to determine the clinical features of pulmonary (PC) and extrapulmonary cryptococcosis (EPC) and compared them among populations with different immune statuses to support appropriate clinical management of this public health threat.
All cases were reported by 14 tertiary teaching hospitals in Jiangsu Province, China from January 2013 to December 2018. The trends in incidence, demographic data, medical history, clinical symptoms, laboratory test indicators, imaging characteristics and diagnostic method of these patients were then stratified by immune status, namely immunocompetent (IC, patients with no recognized underlying disease or those with an underlying disease that does not influence immunity, such as hypertension), mild-to-moderate immunodeficiency (MID, patients with diabetes mellitus, end-stage liver or kidney disease, autoimmune diseases treated with low-dose glucocorticoid therapy, and cancer treated with chemotherapy) and severe immunodeficiency (SID, patients with acquired immunodeficiency syndrome, haematologic malignancies, solid organ transplantation or haematologic stem cell transplantation, idiopathic CD4 lymphocytosis, agranulocytosis, aggressive glucocorticoid or immunosuppressive therapy and other conditions or treatments that result in severe immunosuppression).
The clinical data of 255 cryptococcosis patients were collected. In total, 66.3% of patients (169) were IC, 16.9% (43) had MID, and 16.9% (43) had SID. 10.1% of the patients (17) with IC were EPC, 18.6% of the patients (8) with MID were EPC, and 74.4% of patients (32) were EPC (IC/MID vs. SID, p < 0.001). Fever was more common in the SID group than in the IC and MID groups (69.8% vs. 14.8% vs. 37.2%, p < 0.001). Of chest CT scan, most lesions were distributed under the pleura (72.7%), presenting as nodules/lumps (90.3%) or consolidations (10.7%). Pleural effusion was more common in SID group compared to IC group (33.3% vs. 2.4%, p < 0.001). Positivity rate on the serum capsular polysaccharide antigen detection (CrAg) test was higher in the SID group than in the other two groups [100.0% vs. 84.4% (MID) vs. 78.2% (IC), p = 0.013]. Positivity rate on the serum CrAg test was also higher in cryptococcal meningitis patients than in PC patients (100.0% vs. 79.5%, p = 0.015).
The clinical presentation of MID patients is intermediate between SID and IC patients and is similar to that of IC patients. The serum CrAg test is more sensitive for the identification of SID or EPC patients.
The incidence of cryptococcosis in kidney transplant recipients and acquired immunodeficiency syndrome (AIDS) patients is 10.59/10,00 per year. There are one million cases of cryptococcal meningitis globally per year [1, 2]. Another study found that 32.7% of patients with cryptococcosis had no recognized underlying diseases . An increasing incidence of pulmonary cryptococcosis (PC) has been identified in immunocompetent patients [4,5,6].
With regard to Cryptococcus infection, cell-mediated immunity is the predominant defense and is mainly based on Cryptococcus-specific Th1-type CD4+ T cells that produce interleukin-2 (IL-2), tumour necrosis factor (TNF) and interferon (IFN) . A Th1–Th17 cytokine profile is associated with increased phagocytic activity and inhibition of the growth of Cryptococcus . Our previous study revealed that patients with CD4 T lymphocyte cell counts greater than 378/µL were more likely to be asymptomatic and had a lower mortality rate than those with lower CD4+ T lymphocyte counts [8, 9]. Similarly, another study confirmed that patients with CD4+ T lymphocyte counts lower than 400/μL were prone to disseminated cryptococcosis . The mortality rate in patients with low levels of CD4+ T lymphocytes was significantly higher than that in patients with normal CD4+ T lymphocyte levels [10, 11]. These reports indicated that immune status significantly influences the clinical features and outcomes of cryptococcosis.
Previous studies have mainly focused on the features of cryptococcal meningitis in severe immunocompromised patients, especially the AIDS population [12, 13]. Few studies have compared the clinical features and the performance of diagnostic methods of cryptococcosis among patients with different immune statuses in one study. The 2010 Infectious Diseases Society of America (IDSA) guidelines recommended managing cryptococcosis patients differently only based on whether they were immunocompetent or severely immunocompromised, such as AIDS and transplant patients. However, there are many patients with mild-to-moderate immunodeficiency for various underlying diseases in the clinic.
The CrAg test is playing an increasingly important role in clinical practice. According to the 2019 Revision and Update of the Consensus Definitions of Invasive Fungal Disease from the European Organization for Research and Treatment of Cancer and the Mycoses Study Group Education and Research Consortium (EORTC/MSG), a positivity test for CrAg can serve as confirmatory evidence in the diagnosis of cryptococcosis. This greatly improves the diagnostic status of serum CrAg detection.
However, previous studies mostly focused on the population with severe immunodeficiency, and few studies on the patients with immunocompetency and mild-to-moderate immunodeficiency [4, 14]. The sensitivity of CrAg in patients with different immune states remains to be further explored.
Are the clinical characteristics of mild-to-moderate immunodeficiency patients more similar to immunocompetent patients or severe immunodeficiency patients? So, based on clinical practice, we conducted this multicentre study and compared the clinical features of patients with different immune statuses.
This study compared the clinical characteristics and the value of the CrAg test in PC and EPC patients who were immunocompetent or immunodeficient (mild-to-moderate or severe immunodeficiency).
Proven cryptococcosis cases were reported by 14 tertiary teaching hospitals in Jiangsu Province, China from January 2013 to December 2018. To determine the influence of immune status on the clinical manifestations and diagnostic performance of the CrAg test, patients were carefully evaluated and divided into three groups: the immunocompetent group (IC group), mild-to-moderate immunodeficiency group (MID group) and severe immunodeficiency group (SID group). The patients were also grouped based on whether they had PC or EPC (mainly cryptococcal meningitis). The trend in the incidence and the demographic data, medical history, clinical symptoms, laboratory tests, imaging characteristics and diagnostic methods were analysed and compared (see Fig. 1). The Ethics Committee of Jinling Hospital approved the research protocol. The need of informed consent was waived by the Ethics Committee of Jinling Hospital. None of the data could be traced back to an identifiable patient.
Criteria for diagnosis and grouping
Diagnostic and inclusion criteria
Patients with indicative clinical and imaging manifestations, positive test results for cryptococcal capsular polysaccharide antigen (the name of the kit: CrAg LFA, CRYPTOCOCCAL ANTIGEN LATERAL FLOW ASSAY; the name of the company/manufacturer: IMMY-2701 Corporate Centre Dr Norman Oklahoma 73069 USA—(405) 360–4669; REF: CR2003) in the peripheral blood or cerebrospinal fluid (CSF), or evidence on histopathologic biopsy, or positive results of culture or microscopic examinations .
Patients with co-infections with other pathogens were excluded.
1) Immune status:
IC patients with no recognized underlying disease or those with an underlying disease that does not influence immunity, such as hypertension.
MID patients with diabetes mellitus, end-stage liver or kidney disease, autoimmune diseases treated with low-dose glucocorticoid therapy, and cancer treated with chemotherapy.
SID patients with AIDS, haematologic malignancies, solid organ transplantation or haematologic stem cell transplantation, idiopathic CD4 lymphocytosis, agranulocytosis, aggressive glucocorticoid or immunosuppressive therapy and other conditions or treatments that result in severe immunosuppression.
The standard of low-dose glucocorticoid is less than 20 mg of prednisone per day, and the cumulative dose is less than 700 mg within 3 weeks before enrollment.
2) Pulmonary and extrapulmonary cryptococcosis:
PC Lesions were confined to the lung, no dissemination.
EPC Cryptococcal meningitis or cryptococcemia, with or without pulmonary cryptococcosis.
SPSS 26.0 (SPSS Inc., Chicago, IL, USA) were used to perform the statistical analysis and generate the charts in this study. The independent sample T-test was used for continuous variables with normal distributions, and the results are expressed as the means ± standard deviations. The Mann–Whitney test was used for continuous variables with non-normal distributions, and the results are expressed as the medians and IQRs (interquartile ranges). Univariate analysis of variance and the Brown-Forsythe, Welch and Kruskal–Wallis tests were used for multiple groups. The chi-square test and Fisher’s exact test were used for categorical variables. P < 0.05 was considered statistically significant, and logistic regression was used as a multivariate analysis to determine the risk factors.
Six patients with co-infections were excluded (aspergillosis, n = 2; Mycobacterium tuberculosis, n = 1; Klebsiella pneumoniae, n = 1; Staphylococcus aureus pneumonia, n = 1; mycobacterium complex [MAC], n = 1). Finally, 255 patients with confirmed cases were enrolled in the study. The number of newly proven cases are on the rise overall (24, 29, 48, 41, 58 and 55 from 2013 to 2018, respectively) (see Fig. 2).
In total, 66.3% of the patients with proven cases (169) were IC, 16.9% (43) were MID, and 16.9% (43) were SID. Of the patients with confirmed cases, 62.7% were males. The mean age was 46.6 ± 13.7 years. Patients in the SID group had a lower body mass index (BMI) [20.2 ± 2.4 kg/m2 vs. 23.8 ± 3.0 kg/m2 (IC) vs. 24.3 ± 3.4 kg/m2 (MID), p < 0.001], although there was no significant difference between the IC and MID groups. Only 6.3% of the patients had a clear history of exposure to bird or pigeon droppings before onset.
Overall, 77.6% (198) of the patients had PC, and 22.4% (57) had EPC. In the IC group, 89.9% of the patients (152) had PC, and 10.1% of the patients (17) had EPC. In the MID group, 81.4% of the patients (35) had PC, and 18.6% of the patients (8) had EPC. However, in SID group, the majority of patients (74.4%, 32 cases) were EPC, and 25.6% of the patients (11) were PC. There was no significant difference in the proportion of patients with MID between the PC and EPC groups (17.2% vs. 15.9%, p = 0.806).
The common underlying diseases in MID group were diabetes (46.5%), receiving low-dose glucocorticoid therapy (25.6%), liver dysfunction (18.6%), chemotherapy (14.0%), autoimmune diseases (14.0%), other renal disease (4.7%) and haemopathy (2.3%) respectively (see Table 1).
The clinical symptoms of cryptococcosis are shown in Fig. 3.
Overall, 27.8% (71/255) of the patients had a fever, and the difference among the IC, MID, and SID groups was statistically significant (14.8% vs. 37.2% vs. 69.8%, p < 0.001). Fever was more common in EPC patients than in PC patients (75.4% vs. 14.1%, p < 0.001).
In total, 23.1% (59/255) of the patients presented as asymptomatic, without significant difference in the proportions among the groups [27.2% (IC) vs. 14.0% (MID) vs. 16.3% (SID), p = 0.093]. The proportion of patients with asymptomatic infection was higher in the PC group than in the EPC group (27.3% vs. 8.8%, p = 0.005) (see Table 2). The proportion of patients with headache was 88.2% in the group with cryptococcal meningitis and 3.0% in PC patients.
Patients in the SID group had lower levels of haemoglobin and albumin than the patients in the other groups (p < 0.001). Inflammatory markers were slightly elevated in the SID group (C-reactive protein, procalcitonin), although there were no significant differences between the IC and MID groups. The mean white blood cell were in the normal range.
The lymphocyte count in the total population was 1.7 ± 0.9 × 109/L, 2.1 ± 0.8 × 109/L in IC group, 1.5 ± 0.7 × 109/L in MID group, and 0.7 ± 0.4 × 109/L in SID group. The difference between the two groups was statistically significant (P < 0.001) (see Table 3).
The distribution of lesions was classified as solitary (27.5%, 70), multiple (65.5%, 167) or diffuse (7.1%, 18). A subpleural distribution was predominant in all three groups (IC group 72.8% vs. MID group 64.7% vs. SID group 83.3%, p = 0.292), and the remainder were near the hilar or medial belt (see Table 4). The morphology of PC lesions was mainly nodules/lumps (90.3%) (see Fig. 4).
We present several representative imaging findings in Fig. 5.
Subpleural nodules were dominant in the IC group, while consolidation shadows and cavities were found in MID group, and more irregular mass shadows and large-scale consolidation shadows were found in SID group.
Smear microscopic examination
The positivity rate of peripheral blood smear microscopic examination in patients with cryptococcosis was 4.5% (3/66). The positive cases in IC, MID and SID groups accounted for 0/21, 0/15 and 3/30 (10.0%) respectively. In patients with cryptococcal meningitis, the positivity rate of cerebrospinal fluid smear microscopic examination was 68.6% (35/51), and positivity rates in IC, MID and SID groups were 35.3% (6/17), 6/8 and 88.5% (23/26) [P < 0.001 (SID vs. IC)] (see Table 5).
The positivity rate of the serum CrAg test in the SID group was higher than those in the other two groups [100.0% vs. 84.4% (MID) vs. 78.2% (IC), p = 0.013]. There was no significant difference between IC and MID group. Among patients with cryptococcal meningitis, the positivity rates of the CSF CrAg test were 100.0%, 87.5%, and 100.0% in the IC, MID and SID groups, respectively (p = 0.094), and the positivity rates of the serum CrAg test were 100.0% whatever the immune status. The positivity rate of the serum CrAg test was also higher in cryptococcal meningitis patients than in PC patients (100.0% vs. 79.5%, p = 0.015) (see Table 6).
In this study, 174 patients underwent lung histological examination, including 130 cases of percutaneous lung puncture, 31 cases of surgical pneumonectomy, and 13 cases of transbronchial lung biopsy (TBLB), with positivity rates of 90.0% (117/130), 100% (31/31), and 46.1% (6/13), respectively (see Table 5).
The number of newly diagnosed cases of cryptococcosis in Jiangsu Province is on the rising. Most of them are patients with immunocompetency. We analyzed the reasons as follows:
Firstly, the sensitivity of serum CrAg test was high compared with galactomannan and 1-3-β-d-glucan test. The serum sensitivity of patients with normal immune function was 78.2%. A study concluded that the positivity rate for CrAg in the serum was 80.3% in IC hosts . The CrAg test is playing an increasingly important role in clinical practice. According to the 2019 EORTC/MSG, a positivity test for CrAg can serve as confirmatory evidence in the diagnosis of cryptococcosis. This greatly improves the diagnostic status of serum CrAg detection. It is widely used as a routine screening for suspected lung infections. With advancements in detection technology and improvements in clinical diagnostic methods, an increasing number of cases of cryptococcosis with immunocompetency have been discovered .
Secondly, minimally invasive techniques such as percutaneous pulmonary puncture are gaining popularity. Immunocompetent patients without CNS/bloodstream/skin involvement were more likely to present as asymptomatic, and lesions were often found on chest CT scan by physical examination . In our study, 27.2% patients presented with asymptomatic infection. In the past, we usually followed up these patients, and the diagnosis was made when patients with immunocompromised immune system developed extrapulmonary spread or presented with respiratory or systemic symptoms. We can now diagnose early with techniques like percutaneous lung puncture or tracheoscopy. At this stage, the majority of patients are with immunocompetency.
In addition, it is related to the increased understanding and diagnostic awareness of clinicians in recent years. It could also have something to do with the increased incidence of the disease itself.
In this study, 77.6% of patients had PC, and only 16.9% of patients had SID. This is inconsistent with the fact that the majority of previously reported cases were CNS Cryptococcus infections. A 10-year (2008–2017) retrospective study from western China concluded that most patients with cryptococcosis were immunocompromised (69.1%, 94/136), and the proportions of patients who were immunocompromised were 55.8% (48/86) in the non-disseminated and 92.0% (46/50) in the disseminated groups, respectively . Another report from Chicago also stated that cryptococcal meningitis was identified in 69.1% of HIV-infected patients, 34.4% of non-HIV-infected, nontransplant patients, and 41.9% of solid organ transplant patients .
Cryptococcus spores are inhaled primarily through the respiratory tract [7, 20,21,22]. They accumulate in the alveoli, causing lung infections and then spreading to the central nervous system, bones, skin, prostate and other organs. This also explains why in our study, the number of patients with PC was significantly higher than that with EPC.
After the disease, immunodeficient patients cannot produce enough cytokines such as IL-2 and tumor necrosis factor to confine the disease to the lung, and Cryptococcus spores may spread with bloodstream and lymph nodes. The most common site of infection is the central nervous system, which may be caused by the lack of Cryptococcus capsular antibody in CSF, the lack of complement activation system against the capsule, the dopamine in CSF conducive to the growth of Cryptococcus, and may also be related to the increase of the permeability of the tight connection and the destruction of the integrity of the blood–brain barrier .
Patients with SID were most likely to be EPC, followed by patients with MID and IC. When extrapulmonary spread occurs, CrAg sensitivity in serum and CSF can reach almost 100%. Patients with high load of Cryptococcus pathogens and high antigen concentration in blood are easy to be detected, which is conducive to rapid and definite diagnosis. However, for people with IC and MID, in order to prevent missed diagnosis, negative results cannot completely exclude the diagnosis, and the patient's immune status should be combined.
We conducted a multi-factor analysis to found that patients with severe immune deficiency, headache symptom are independent risk factors for the development of disseminated. But the Odd Ratio (OR) values and confidence intervals (CI) are large. We analyzed the possible reasons as follows: 1. the proportion of patients with PC and EPC was too large, and the sample size of patients with EPC was small; 2. the observational indicators, especially headache symptoms, were significantly correlated with the outcome and the effect size was large, so the OR value and CI were large. When patients with PC are combined with severe immunodeficiency, headache, central nervous system infection should be considered, and timely lumbar puncture should be performed.
Based on the above results, more severely immunodeficient patients are more likely to develop a fever. Similarly, EPC patients were significantly more likely to have a fever than PC patients (75.4% vs 14.1%, p < 0.001), and this result was consistent with a study from Western China (50.0% vs 23.2%, p = 0.001) [14, 25, 26]. We believe that when the immunodeficiency is aggravated, the body does not produce a strong immune response and enough cytokine, like interleukin-2 against Cryptococcus infection. Then the pathogen load is high in the body and produce more endogenous pyrogen, through blood circulation effects on the temperature regulating center and change its function, cause fever reaction.
We observed that inflammatory markers, such as CRP protein and PCT, were normal in IC and MID patients and slightly elevated in the SID group. White blood cell were essentially normal in all groups. This suggests that normal inflammatory indicators do not exclude pulmonary cryptococcosis. On the other hand, in the diagnosis and differential diagnosis of disease, if the patient's inflammatory indicators are significantly increased, the presence of other pathogen infection should be further considered.
Multiple subpleural nodules/lumps or consolidations are important imaging features of PC. Patients with SID were more likely to have pleural effusion in this study. These imaging findings have a degree of specificity compared to other pulmonary infections. This also explains why percutaneous lung biopsy is used in most pathological examinations, and the positive rate of percutaneous lung biopsy (90.0%) is much higher than that of TBLB (46.1%). These are closely related to the characteristics of cryptocosis in which the lesions are mostly located in subpleural [12, 16, 27, 28].
The positivity rate of traditional smear microscopic examination was lower than that for the serum CrAg test. However, in cryptococcal meningitis patients with SID, the positivity rate reached 88.5% in CSF, which is nearly similar to the 85% reported in meningitis patients . Therefore, patients with suspected cryptococcal meningitis should be examined by lumbar puncture as soon as possible to obtain a CSF specimen for testing [30, 31].
This study, which uses underlying disease to divide patients into different immune groups, does not seem objective. Part of cases in our study were retrospective, lacking some objective indicators, and there is no single objective indicator to distinguish the systemic immune status of patients. Furthermore, we analyzed the peripheral blood lymphocyte counts of patients and found that the difference in peripheral blood lymphocyte counts between different groups was statistically significant. This also confirms that the classification method we use for underlying diseases is relatively reliable and close to the clinic to facilitate rapid judgment by clinicians. In future studies, if objective immune indicators were used to group patients, such as CD4+ T lymphocyte cell count, it might bring us more valuable information.
The clinical presentation of MID patients is intermediate between those of SID and IC patients and is similar to those of IC patients in many respects. The serum CrAg test is relatively more sensitive in SID or EPC patients.
Availability of data and materials
The datasets during and/or analysed during the current study are available from the corresponding author on reasonable request.
Capsular polysaccharide antigen
Acquired immunodeficiency syndrome
Tumor necrosis factor
Body mass index
Infectious Diseases Society of America
European Organization for Research and Treatment of Cancer and the Mycoses Study Group Education and Research Consortium
White blood cells
- APACHE II:
Acute physiology and chronic health evaluation
Bronchoalveolar lavage fluid
Transbronchial lung biopsy
Central nervous system
Chen YT, Lee WS, Tsai CA, Fan WC, Wu PF, Wang FD. Incidence of and risk factors for cryptococcosis in kidney transplant recipients in Taiwan-A nationwide population-based study. Int J Infect Dis. 2019;88:154–8.
Gullo FP, Rossi SA, Sardi Jde C, Teodoro VL, Mendes-Giannini MJ, Fusco-Almeida AM. Cryptococcosis: epidemiology, fungal resistance, and new alternatives for treatment. Eur J Clin Microbiol Infect Dis. 2013;32(11):1377–91.
Fang LF, Zhang PP, Wang J, Yang Q, Qu TT. Clinical and microbiological characteristics of cryptococcosis at an university hospital in China from 2013 to 2017. Braz J Infect Dis. 2020;24(1):7–12.
Liu K, Ding H, Xu B, You R, Xing Z, Chen J, Lin Q, Qu J. Clinical analysis of non-AIDS patients pathologically diagnosed with pulmonary cryptococcosis. J Thorac Dis. 2016;8(10):2813–21.
Hou X, Kou L, Han X, Zhu R, Song L, Liu T. Pulmonary cryptococcosis characteristics in immunocompetent patients-A 20-year clinical retrospective analysis in China. Mycoses. 2019;62(10):937–44.
Deng H, Zhang J, Li J, Wang D, Pan L, Xue X. Clinical features and radiological characteristics of pulmonary cryptococcosis. J Int Med Res. 2018;46(7):2687–95.
Dos Santos VM. Pulmonary cryptococcosis. Arch Iran Med. 2019;22(10):629–30.
He Q, Ding Y, Zhou W, et al. Clinical features of pulmonary cryptococcosis among patients with different levels of peripheral blood CD4+ T lymphocyte counts. BMC Infect Dis. 2017;17(1):768.
Thornton CS, Larios O, Grossman J, Griener TP, Vaughan S. Pulmonary Cryptococcus infections as a manifestation of idiopathic CD4 lymphocytopenia: case report and literature review. BMC Infect Dis. 2019;19(1):862.
Ding Y, Li P, He Q, Wei H, Wu T, Xia D, Tan M, Shi Y, Su X. The CD4+ T-lymphocyte count is an important predictor for the prognosis of cryptococcosis. Eur J Clin Microbiol Infect Dis. 2017;36(5):897–904.
Mukaremera L, Nielsen K. Adaptive immunity to Cryptococcus neoformans infections. J Fungi. 2017;3:64.
Hu Z, Chen J, Wang J, et al. Radiological characteristics of pulmonary cryptococcosis in HIV-infected patients. PLoS ONE. 2017;12(3):e0173858.
Fujioka K, Nagai T, Kinoshita Y, et al. Successful treatment with voriconazole combined with amphotericin B-liposome for fluconazole-resistant pulmonary cryptococcosis after renal transplantation. CEN Case Rep. 2019;8(4):261–5.
Qu J, Zhang X, Lu Y, Liu X, Lv X. Clinical analysis in immunocompetent and immunocompromised patients with pulmonary cryptococcosis in western China. Sci Rep. 2020;10(1):9387.
Donnelly JP, Chen SC, Kauffman CA, et al. Revision and update of the consensus definitions of invasive fungal disease from the European Organization for research and treatment of cancer and the mycoses study group education and research consortium. Clin Infect Dis. 2020;71(6):1367–76.
Min J, Huang K, Shi C, et al. Pulmonary Cryptococcosis: comparison of Cryptococcal antigen detection and radiography in Immunocompetent and Immunocompromised patients. BMC Infect Dis. 2020;20(1):91.
Zhou Y, Lin PC, Ye JR, et al. The performance of serum cryptococcal capsular polysaccharide antigen test, histopathology and culture of the lung tissue for diagnosis of pulmonary cryptococcosis in patients without HIV infection. Infect Drug Resist. 2018;11:2483–90.
Xie X, Xu B, Yu C, Chen M, Yao D, Xu X, Cai X, Ding C, Wang L, Huang X. Clinical analysis of pulmonary cryptococcosis in non-HIV patients in south China. Int J Clin Exp Med. 2015;8(3):3114–9.
Perfect JR, Dismukes WE, Dromer F, Goldman DL, et al. Clinical practice guidelines for the management of cryptococcal disease: 2010 update by the infectious diseases society of America. Clin Infect Dis. 2010;50(3):291–322.
Setianingrum F, Rautemaa-Richardson R, Denning DW. Pulmonary cryptococcosis: a review of pathobiology and clinical aspects. Med Mycol. 2019;57(2):133–50.
Velagapudi R, Hsueh YP, Geunes-Boyer S, Wright JR, Heitman J. Spores as infectious propagules of Cryptococcus neoformans. Infect Immun. 2009;77:4345–55.
Zavala S, Baddley JW. Cryptococcosis. Semin Respir Crit Care Med. 2020;41(1):69–79.
Rajesh V, Yen-Ping H, Scarlett G-B, et al. Spores as infectious propagules of Cryptococcus neoformans. Infect Immun. 2009;77:4345–55.
Vilchez RA, Irish W, Lacomis J, Costello P, Fung J, Kusne S. The clinical epidemiology of pulmonary cryptococcosis in non-AIDS patients at a tertiary care medical center. Medicine (Baltimore). 2001;80(5):308–12.
Wang D, Wu C, Gao J, et al. Comparative study of primary pulmonary cryptococcosis with multiple nodules or masses by CT and pathology. Exp Ther Med. 2018;16(6):4437–44.
He Q, Ding Y, Zhou W, Li H, Zhang M, Shi Y, Su X. Clinical features of pulmonary cryptococcosis among patients with different levels of peripheral blood CD4+ T lymphocyte counts. BMC Infect Dis. 2017;17(1):768.
Liang L, Cong P, Wang Y, Liang Z. Clinical and radiological features of patients with pulmonary cryptococcosis in a hospital of North China. Cureus. 2020;12(5):e8061.
Xie LX, Chen YS, Liu SY, Shi YX. Pulmonary cryptococcosis: comparison of CT fndings in immunocompetent and immunocompromised patients. Acta Radiol. 2015;56:447–53.
Takazono T, Saijo T, Ashizawa N, et al. Clinical features and cause analysis of false positive results of Aspergillus galactomannan assay in pulmonary cryptococcosis patients. Eur J Clin Microbiol Infect Dis. 2019;38(4):735–41.
Rajasingham R, Wake RM, Beyene T, Katende A, Letang E, Boulware DR. Cryptococcal meningitis diagnostics and screening in the era of point-of-care laboratory testing. J Clin Microbiol. 2019;57(1):e01238-e1318.
George IA, Spec A, Powderly WG, Santos CAQ. Comparative epidemiology and outcomes of human immunodeficiency virus (HIV), non-HIV non-transplant, and solid organ transplant associated cryptococcosis: a population-based study. Clin Infect Dis. 2018;66(4):608–11.
Thanks to AJE for providing language assistance for this article.
This work was supported by the Project of Natural Science Foundation of China (82070011, 81873400), the Key Project of Jiangsu Commission of Health (K2019004), and the “333 project” of Jiangsu Province (BRA2019339).
Ethics approval and consent to participate
All methods were carried out in accordance with Declaration of Helsinki. The Ethics Committee of Jinling Hospital approved the research protocol. The need of informed consent was waived by the Ethics Committee of Jinling Hospital. None of the data could be traced back to an identifiable patient.
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Wang, Y., Gu, Y., Shen, K. et al. Clinical features of cryptococcosis in patients with different immune statuses: a multicenter study in Jiangsu Province–China. BMC Infect Dis 21, 1043 (2021). https://doi.org/10.1186/s12879-021-06752-x
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