scholarly journals Living Bacterial Microneedles for Fungal Infection Treatment

Research ◽  
2020 ◽  
Vol 2020 ◽  
pp. 1-9 ◽  
Author(s):  
Fengyuan Wang ◽  
Xiaoxuan Zhang ◽  
Guopu Chen ◽  
Yuanjin Zhao

Fungal infections are everlasting health challenges all over the world, bringing about great financial and medical burdens. Here, inspired by the natural competition law of beneficial bacteria against other microbes, we present novel living microneedles (LMNs) with functionalized bacteria encapsulation for efficient fungal infection treatment. The chosen beneficial bacterial components, Bacillus subtilis (B. subtilis), which are naturally found on the human skin and widely used for food processing, can get nutrients from the skin and escape from the immune system with the help of microneedles. Besides, the encapsulated B. subtilis can continuously produce and secrete various potential antifungal agents which can directly bind to fungal cell surface-associated proteins and destruct the cell membranes, thus avoiding drug resistance. After immobilization in the LMNs, the bacteria can stay within the LMNs without invasion and the encapsulated bacteria together with microneedles can be removed after application. Thus, the side effects, especially the risk for subsequent bacterial infections, are controlled to a minimum to ensure security. In addition, strong penetrability of the microneedles enhances penetration of antifungal agents, and their heights can be adjusted according to the infected depth to acquire better therapeutic effects. These features make the LMNs potentially valuable for clinical applications.

2003 ◽  
Vol 10 (5) ◽  
pp. 882-885 ◽  
Author(s):  
Justin Digby ◽  
John Kalbfleisch ◽  
Andy Glenn ◽  
Angie Larsen ◽  
William Browder ◽  
...  

ABSTRACT Fungal infections in the critically ill patient are difficult to diagnose and are associated with a high mortality rate. A major obstacle to managing fungal infection is the lack of a reliable clinical assay that will rapidly identify patients with fungal sepsis. Glucans are polymers of glucose that are found in the cell wall of fungi and certain bacteria. Glucans are also released from the fungal cell wall into the extracellular milieu. Several studies have reported that detection of fungal glucan in serum or plasma is useful in the diagnosis of mycoses. However, recent studies have questioned the clinical utility of this assay. In this study, we examined serum glucan levels in intensive care unit (ICU) patients and attempt to correlate serum glucan levels with the presence of fungal infection. Following attainment of informed consent, serum was harvested from 46 ICU patients with confirmed fungal infections, confirmed bacterial infections, or no evidence of infection. Sera from eight healthy volunteers served as control. Serum glucan was assayed with a glucan-specific Limulus assay. Serum glucan levels were increased (69.6 ± 17 pg/ml; P < 0.001) in ICU patients versus the normal (11.5 ± 1.3 pg/ml) and noninfected ICU (27.4 ± 17 pg/ml) controls. However, serum glucan levels were not different in patients with confirmed fungal infections versus those with confirmed bacterial infections. Thus, serum glucan levels did not show a correlation with the presence of fungal infections and do not appear to be specific for fungal infections. However, the assay may be useful as a negative predictor of infection.


Blood ◽  
2008 ◽  
Vol 112 (11) ◽  
pp. 4374-4374
Author(s):  
Aj ay Sharma ◽  
Velu Nair ◽  
Satyaranjan Das ◽  
Deepak Kumar Mishra ◽  
Jyoti Kotwal ◽  
...  

Abstract Background: Hematopoeitic stem cell transplantation (HSCT) is the standard of care in a large number of disorders for over three decades all over the world. Despite significant improvements in conditioning protocols, the mortality still remains significantly high and peri-transplant infections continue to be a big challenge. A number of regimens for primary prophylaxis against various infections are being used during conditioning with varying success in reducing the incidence of infections. But it might result in increasing incidence of resistant infections besides increasing the transplant cost. Objectives: To evaluate the impact of infection prophylaxis upon infection related mortality in allo-HSCT. Materials and Methods: We analyzed the data of 96 consecutive stem cell transplants performed in our centre between 1998 and 2006. We did not use any prophylaxis for bacterial or fungal infections in these cases. A total of 86 patients underwent HSCT for various indications at our 3 bedded bone marrow transplantation unit (BMTU). The mean age was 24 years (range: 2–45). The indications for allogeneic transplants were CML: 28, AML: 8, ALL: 5, CLL: 1, MDS: 1, Thalassemia major: 12, PRCA: 1 and Aplastic/Fanconi’s anemia: 4. The indications for autologous transplants included multiple myeloma (15), NHL (8), AML(7) and solid tumors (5) Allogeneic transplants were performed with full HLA matched siblings. The conditioning was done with standard Busulfan-Cyclophosphamide (Bu-Cy) based protocols for leukemia; Fludarabine, Cyclophosphamide & ATG for PRCA and aplastic anemia and Bu-Cy-ATG for thalassemia. The median cell dose was 6.8 × 108 (range: 2.7–11.7) MNC/Kg. The median day of engraftment (ANC &gt; 500/mm3) was day 10 (range 7–20). None of the patients received primary prophylaxis with any antibiotics or antifungal agents during conditioning. Patients who developed neutropenic fever or the evidence of bacterial or fungal infections were treated with empirical therapy based on our hospital infection policy based antimicrobial protocols. Results: A total of 64 patients developed documented infections. Amongst these the positive bacteriological cultures were obtained from blood (64%) followed by urine (12%), sputum (8%) and catheter related infections (5%) The antibiotics were changed if specific organism could be identified. Antifungal agents were started empirically if fever continued 48 hours after initiation of initial antibiotics even if no causative agent was identified. 78 (92 %) patients required antibiotics. Total 38 patients had documented bacterial infections. The majority of bacterial infections (56%) occurred in the first 30 days following SCT. The organisms identified were mainly Gram negative bacteria (77% e.g, E Coli-68%, Pseudomonas aeroginosa-13%, Enterobacter-2%, Klebsiella pneumoniae-2%) with a few gram positive organisms (23%). The gram positive organisms were Staphylococcus aureus (13%) and Coagulase negative staphylococcus (8%). 05 patients developed septicemia with fatal multi-organ failure. The 100 day mortality due to infections has been 9 (9.2 %) and one year infection related mortality was 13%. This rate of infections was not significantly higher as compared to he rates when antibiotics & antifungals were used as prophylaxis Fungal infections were documented in 19 patients(Candida: 57%, Aspergillus: 33% and Zygomycetes: 10%) Conclusion: The study demonstrates that adherence to a well planned infection control strategy for transplant units and strict preventive measures can ensure a low incidence of infections with success rates comparable to any developed country. Although the number is small to make any definite conclusion, there is a feasibility of avoiding prophylactic use of antibiotics in conditioning regimens, thereby, decreasing the risk of resistant infections besides bringing down the cost of transplant procedure which has a great bearing on the availability of transplant to all eligible patients in a country like India where affordability is restricted greatly by cost factors.


Biomedicines ◽  
2021 ◽  
Vol 9 (5) ◽  
pp. 536
Author(s):  
Hiroshi Tamura ◽  
Johannes Reich ◽  
Isao Nagaoka

The blue blood of the horseshoe crab is a natural, irreplaceable, and precious resource that is highly valued by the biomedical industry. The Limulus amebocyte lysate (LAL) obtained from horseshoe crab blood cells functions as a surprisingly sophisticated sensing system that allows for the extremely sensitive detection of bacterial and fungal cell-wall components. Notably, LAL tests have markedly contributed to the quality control of pharmaceutical drugs and medical devices as successful alternatives to the rabbit pyrogen test. Furthermore, LAL-based endotoxin and (1→3)-β-D-glucan (β-glucan) assay techniques are expected to have optimal use as effective biomarkers, serving as adjuncts in the diagnosis of bacterial sepsis and fungal infections. The innovative β-glucan assay has substantially contributed to the early diagnosis and management of invasive fungal diseases; however, the clinical significance of the endotoxin assay remains unclear and is challenging to elucidate. Many obstacles need to be overcome to enhance the analytical sensitivity and clinical performance of the LAL assay in detecting circulating levels of endotoxin in human blood. Additionally, there are complex interactions between endotoxin molecules and blood components that are attributable to the unique physicochemical properties of lipopolysaccharide (LPS). In this regard, while exploring the potential of new LPS-sensing technologies, a novel platform for the ultrasensitive detection of blood endotoxin will enable a reappraisal of the LAL assay for the highly sensitive and reliable detection of endotoxemia.


Author(s):  
Ergüden Bengü

Although there are innovations in the treatment of diseases caused by fungi and medicines with multiple targets have been developed, the search for a drug with a broad spectrum and without any side effects continues to date. It is generally accepted that determining the cellular target responsible for the toxic effect opens up new possibilities for the development of new drugs. Especially the effects of antifungal agents on the surface components of the fungal cell, on cell wall synthesis and the identification of the target site are crucial in antifungal drug development. Thus studies on the fungal cell membranes in connection with the antifungal agents, aim to develop new strategies for the therapy of fungal infections. Antifungal agents targeting fungal cell wall and cell membrane components have increased in importance in clinical studies. In this study, understanding the mechanism of action of benzyl alcohol, a known membrane fluidizer, and the determination of its cellular targets are aimed. We have shown that in the presence of sorbitol, the osmotic stabilizer, benzyl alcohol becomes less effective against yeast cell. Moreover, benzyl alcohol disrupts cell membrane, causing leakage of ions to the extracellular medium. Nuclear membrane is distorted upon treatment of yeast cells with benzyl alcohol. Thus, we conclude that both outer and inner yeast cell membranes are compromised by the action of benzyl alcohol.


Author(s):  
Spoorthy H. V. ◽  
L. Padma ◽  
Srividya B. P.

Background: In tropical countries like India, superficial fungal infections are quite common and certain infections like tinea is rampantly spreading in epidemic proportions and frequent relapses after treatment have increased the need for long term therapy significantly increasing the cost of treatment, so the treatment of fungal infection can raise economic burden on the patient. The aim of the study was to analyze the cost variation of topical antifungal drugs and oral antifungal drugs of various brands for superficial fungal infection available in India.Methods: Cost in Indian Rupees (INR) of antifungal agents manufactured by different pharmaceutical companies in India was collected from the Current index of medical specialities (CIMS) October to December 2019. Minimum cost, maximum cost, cost ratio, cost variation was calculated.Results: In oral dosage form, fluconazole, Itraconazole show the maximum cost variation. In topical single drug therapy luliconazole, terbinafine show maximum cost variation.Conclusions: There is wide cost variation among antifungal agents available in Indian Market. There is need of strict actions for cost policy regulation and sensitization of doctor for selection of appropriate brand drugs. 


2009 ◽  
Vol 27 (15_suppl) ◽  
pp. e20618-e20618 ◽  
Author(s):  
A. Bonini ◽  
A. Tieghi ◽  
B. Gamberi ◽  
A. Imovilli ◽  
C. Carbonelli ◽  
...  

e20618 Background: Infections are the main complication for neutropenic patients (pts).Fungal infections represent a frequent cause of death. Caspofungin (Caspo) is the first drug able to inhibit the growth of the fungal cell wall. Methods: Since 2004 we began a prospective study with the administration of Caspo as first line therapy in 63 consecutive adult neutropenic pts. With persistent fever despite antibiotics,a chest CT-scan and galactomannan test were performed. In case of probable or proven infection Caspo was administered at the dose of 70 mg on the first day followed by 50 mg daily. They were 35 males and 28 females; the mean age was 56 yrs. The diagnoses were: leukemia 44, myeloma 3, lymphoma 16; the disease's phases were: new onset 24, remission 16, relapse 23. 12 pts received an allogeneic and 6 an autologous transplant; the others received conventional chemotherapy. Results: Fungal infections were proven in 12 and probable in 51 cases.The first site of infection was the lung in 62 pts. CT scan was positive(halo sign or air-crescent sign)in all the pts with a lung localization. BAL was performed in 37 pts.The mean time of treatment was 18 days. Caspo was well tolerated and not discontinued for adverse events. Among pts submitted to an allogeneic HSCT the concomitant therapy with Cyclosporin A was not influenced by Caspo. No adverse events during the infusion were seen, and it was not necessary to administer any premedication. The global (partial and complete) response was 50/63 (79%); 13 pts died for fungal infection. The responses were generally similar for probable and proven infections. No breakthrough infections were seen. All surviving patients, upon discharge from the hospital, received oral treatment with voriconazole. For all the cured pts, there was a concomitant recovery of neutrophils and this seems crucial for the resolution of the infection. Among the 50 responsive patients, 25 died later: 23 for hematologic disease and 2 for sepsis during recurrence of the malignant disease. In 2 pts there was the recurrence of the fungal infection. Conclusions: The resolution rate of the infections is very high; Caspo seems safe, it does not preclude any other treatment, it is well tolerated and the cost is lower than other antifungal treatments. No significant financial relationships to disclose.


2020 ◽  
Vol 38 (8) ◽  
pp. 815-822 ◽  
Author(s):  
Yoshinobu Kanda ◽  
Shun-ichi Kimura ◽  
Masaki Iino ◽  
Takahiro Fukuda ◽  
Emiko Sakaida ◽  
...  

PURPOSE Empiric antifungal therapy (EAT) is recommended for persistent febrile neutropenia (FN), but in most patients, it is associated with overtreatment. The D-index, calculated as the area surrounded by the neutrophil curve and the horizontal line at a neutrophil count of 500/μL, reflects both the duration and depth of neutropenia and enables real-time monitoring of the risk of invasive fungal infection in individual patients at no cost. We investigated a novel approach for patients with persistent FN called D-index–guided early antifungal therapy (DET), in which antifungal treatment is postponed until a D-index reaches 5,500 or the detection of positive serum or imaging tests, and compared it with EAT in this multicenter open-label noninferiority randomized controlled trial. PATIENTS AND METHODS We randomly assigned 423 patients who underwent chemotherapy or hematopoietic stem-cell transplantation for hematologic malignancies to the EAT or DET group. The prophylactic use of antifungal agents other than polyenes, echinocandins, or voriconazole was allowed. Micafungin at 150 mg per day was administered as EAT or DET. RESULTS In an intent-to-treat analysis of 413 patients, the incidence of probable/proven invasive fungal infection was 2.5% in the EAT group and 0.5% in the DET group, which fulfilled the predetermined criterion of noninferiority of the DET group (−2.0%; 90% CI, −4.0% to 0.1%). The survival rate was 98.0% versus 98.6% at day 42 and 96.4% versus 96.2% at day 84. The use of micafungin was significantly reduced in the DET group (60.2% v 32.5%; P < .001). CONCLUSION A novel strategy, DET, decreased the use and cost of antifungal agents without increasing invasive fungal infections and can be a reasonable alternative to empiric or preemptive antifungal therapy.


2015 ◽  
Vol 57 (6) ◽  
pp. 527-530 ◽  
Author(s):  
Graziella Hanna PEREIRA ◽  
Valéria Pereira Barbosa LANZONI ◽  
Elisa Maria BEIRÃO ◽  
Artur TIMERMAN ◽  
Marcia de Souza Carvalho MELHEM

Paracoccidioidomycosis and histoplasmosis are systemic fungal infections endemic in Brazil. Disseminated clinical forms are uncommon in immunocompetent individuals. We describe two HIV-negative patients with disseminated fungal infections, paracoccidioidomycosis and histoplasmosis, who were diagnosed by biopsies of suprarenal lesions. Both were treated for a prolonged period with oral antifungal agents, and both showed favorable outcomes.


Blood ◽  
2014 ◽  
Vol 124 (21) ◽  
pp. 5853-5853
Author(s):  
Deepesh P Lad ◽  
Pankaj Malhotra ◽  
Alka Khadwal ◽  
Gaurav Prakash ◽  
Pallab Ray ◽  
...  

Abstract Introduction: There are evidence based guidelines for the prophylaxis and management of infections in hematopoietic stem cell transplant recipients. However, the infection profile of transplant centers differs from center to center even in different regions of the same country. The reported incidence of bacterial, fungal and viral infections ranges widely from 13-60%, 4-30% and 2-16% respectively across the world. Here we report the infection profile in our transplant center. Methods: This was a retrospective study done at a tertiary care referral center in India. Data of hematopoietic stem cell transplants from 2004 –2014 was analyzed. All recipients received trimethoprim-sulphamethoxazole, levofloxacin, fluconazole and acyclovir prophylaxis. Voriconazole was used in allogeneic transplants after 2011. Definite bacterial infections were defined as any positive cultures from blood, urine, sputum, pus. Definite infective diarrhea was defined as stool culture or Clostridium difficile toxin positivity. Definite fungal infection required confirmation by culture or histopathology. Probable fungal infection required one each of host factors, clinical features and mycological evidence. Possible fungal infection required any one of the above three factors. Antifungals were started on day 3-5 as per the febrile neutropenia guidelines. CMV was monitored by RQ-PCR weekly till 100 days post transplant. All recipients were nursed in HEPA (high efficiency particulate air) filtered rooms till the resolution of infection or engraftment whichever was later. Results: Data of first 100 (36 allogeneic and 64 autologous) transplants was analyzed. All patients except 3 developed fever requiring antibiotics. There were 68 documented bacterial infections in 47 transplant recipients (47%). Gram negative were the most frequent isolates 49/68 (72.1%) followed by Gram positive organisms 19/68 (27.9%). Polymicrobial infections were seen in 11 patients (16.1%). Infections were significantly more common in allogeneic (26/36) than autologous transplant recipients (34/64) (p=0.005). Diarrhea was seen in 59 patients. Clostridium difficile toxin positivity was seen in 7 cases (11.8%). CMV infection was seen in 9 allogeneic HSCT recipients (25%). All patients had ongoing GVHD at the time of CMV reactivation and were on additional immunosuppression with corticosteroids. The diagnosis of fungal infection was made in 54 patients (54%). It was categorized as probable in 10 and possible in 44. Definite fungal infections could not be documented in any case. Antifungals were used for a median duration of 4.5 days (SD ±6.9). Infection attributed mortality was 9%. The median duration of antimicrobial usage was 13 days (SD±9.2). The median duration of total hospital stay was 38 days (SD±31.7). The median day of neutrophil engraftment was 12 days (SD±3.5). Multiple regression analysis revealed duration of antimicrobial use to be associated with hospital stay (p<0.0001). Conclusions: Antimicrobials were used for up to one third of the total hospital stay of HSCT. Bacterial and fungal infections were the major cause for prolongation of the hospital stay in our center. The incidence of possible fungal infections is higher than centers in other parts of the world and signifies the need for alternative detection methods to confirm the diagnosis. Whether the agent, host or environment factor in tropical and developing countries, contributes to this increased risk of infections needs to be evaluated in a prospective study. Disclosures No relevant conflicts of interest to declare.


Author(s):  
Prasad A. Kelkar ◽  
Jyoti V. Hirekerur

<p class="abstract"><strong>Background:</strong> From last few years, the fungal infection has been increasing due to greatly enhanced international traffic and as opportunistic infections in consequence of use of powerful cytotoxic drugs. The disease invariably occurs in diabetics, usually with ketoacidosis, immune compromised patients. Hence, we planned to undertake the present study to evaluate a standard method of management of fungal infections of nose and paranasal sinuses.</p><p class="abstract"><strong>Methods:</strong> A detailed examination of the nose and pranasal sinuses was carried out in the department of ENT. The patients were continuously monitored with pulse oximetry and ECG monitor. In all patients, nasal endoscopy was performed.  </p><p class="abstract"><strong>Results:</strong> In this study, fungal infections of the nose and paranasal sinuses were found to be common between 20 and 50 years of age. Aspergillosis was the commonest sinonasal fungal infection followed by allergic fungal sinusitis, rhinosporidiosis and mucormycosis.</p><p class="abstract"><strong>Conclusions:</strong> Early detection, proper and adequate dose of antifungal agents, timely surgical intervention in the form of debridement and sphenoethmoidectomy and orbital exenteration improve the survival rate in the disease of sinonasal fungal infections.</p><p> </p>


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