scholarly journals Non-invasive messenger RNA transcriptional evaluation in human kidney allograft dysfunction

Author(s):  
G. Joelsons ◽  
T. Domenico ◽  
L.F. Gonçalves ◽  
R.C. Manfro
2010 ◽  
Vol 90 ◽  
pp. 246
Author(s):  
G. Joelsons ◽  
Aquino E.C. Dias ◽  
R. B. Cupertino ◽  
A. Nogare ◽  
L. F.S. Gonçalves ◽  
...  

Pharmaceutics ◽  
2020 ◽  
Vol 13 (1) ◽  
pp. 45
Author(s):  
Iman M. Alfagih ◽  
Basmah Aldosari ◽  
Bushra AlQuadeib ◽  
Alanood Almurshedi ◽  
Mariyam M. Alfagih

Messenger RNA (mRNA)-based vaccines have shown promise against infectious diseases and several types of cancer in the last two decades. Their promise can be attributed to their safety profiles, high potency, and ability to be rapidly and affordably manufactured. Now, many RNA-based vaccines are being evaluated in clinical trials as prophylactic and therapeutic vaccines. However, until recently, their development has been limited by their instability and inefficient in vivo transfection. The nanodelivery system plays a dual function in RNA-based vaccination by acting as a carrier system and as an adjuvant. That is due to its similarity to microorganisms structurally and size-wise; the nanodelivery system can augment the response by the immune system via simulating the natural infection process. Nanodelivery systems allow non-invasive mucosal administration, targeted immune cell delivery, and controlled delivery, reducing the need for multiple administrations. They also allow co-encapsulating with immunostimulators to improve the overall adjuvant capacity. The aim of this review is to discuss the recent developments and applications of biodegradable nanodelivery systems that improve RNA-based vaccine delivery and enhance the immunological response against targeted diseases.


PLoS ONE ◽  
2017 ◽  
Vol 12 (6) ◽  
pp. e0180045 ◽  
Author(s):  
Jung-Woo Seo ◽  
Haena Moon ◽  
Se-Yun Kim ◽  
Ju-Young Moon ◽  
Kyung Hwan Jeong ◽  
...  

Nephron ◽  
1989 ◽  
Vol 53 (4) ◽  
pp. 338-342 ◽  
Author(s):  
H.E. Feucht ◽  
J. Zwirner ◽  
D. Bevec ◽  
Margot Lang ◽  
E. Felber ◽  
...  

2018 ◽  
Vol 104 (6) ◽  
pp. 1229-1239 ◽  
Author(s):  
Youssra Haouami ◽  
Tarak Dhaouadi ◽  
Imen Sfar ◽  
Mongi Bacha ◽  
Tahar Gargah ◽  
...  

2016 ◽  
Vol 2 (9) ◽  
pp. e98
Author(s):  
Ravinder K. Wali ◽  
Heather A. Prentice ◽  
Venkata Reddivari ◽  
Geroge Baffoe-Bonnie ◽  
Cinthia I. Drachenberg ◽  
...  

1997 ◽  
Vol 5 (3) ◽  
pp. 199-203 ◽  
Author(s):  
Angelo M de Mattos ◽  
Mary M Meyer ◽  
Douglas J Norman ◽  
William M Bennett ◽  
Jerald Sprague ◽  
...  

PLoS ONE ◽  
2021 ◽  
Vol 16 (4) ◽  
pp. e0249930
Author(s):  
Aziz Belkadi ◽  
Gaurav Thareja ◽  
Darshana Dadhania ◽  
John R. Lee ◽  
Thangamani Muthukumar ◽  
...  

Kidney transplantation is the treatment of choice for patients with end-stage kidney failure, but transplanted allograft could be affected by viral and bacterial infections and by immune rejection. The standard test for the diagnosis of acute pathologies in kidney transplants is kidney biopsy. However, noninvasive tests would be desirable. Various methods using different techniques have been developed by the transplantation community. But these methods require improvements. We present here a cost-effective method for kidney rejection diagnosis that estimates donor/recipient-specific DNA fraction in recipient urine by sequencing urinary cell DNA. We hypothesized that in the no-pathology stage, the largest tissue types present in recipient urine are donor kidney cells, and in case of rejection, a larger number of recipient immune cells would be observed. Extensive in-silico simulation was used to tune the sequencing parameters: number of variants and depth of coverage. Sequencing of DNA mixture from 2 healthy individuals showed the method is highly predictive (maximum error < 0.04). We then demonstrated the insignificant impact of familial relationship and ethnicity using an in-house and public database. Lastly, we performed deep DNA sequencing of urinary cell pellets from 32 biopsy-matched samples representing two pathology groups: acute rejection (AR, 11 samples) and acute tubular injury (ATI, 12 samples) and 9 samples with no pathology. We found a significant association between the donor/recipient-specific DNA fraction in the two pathology groups compared to no pathology (P = 0.0064 for AR and P = 0.026 for ATI). We conclude that deep DNA sequencing of urinary cells from kidney allograft recipients offers a noninvasive means of diagnosing acute pathologies in the human kidney allograft.


2018 ◽  
Vol 79 (5) ◽  
pp. 343-355 ◽  
Author(s):  
Voravech Nissaisorakarn ◽  
John Richard Lee ◽  
Michelle Lubetzky ◽  
Manikkam Suthanthiran

2019 ◽  
Vol 73 (6) ◽  
pp. A10-A14
Author(s):  
Suwasin Udomkarnjananun ◽  
Somrath Srijaruneruang ◽  
Natavudh Townamchai ◽  
Kroonpong Iampenkhae ◽  
Wipusit Taesombat ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document