Methods and compositions to predict and detect acute rejection

US9746479B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9746479-B2
Application numberUS-201113583750-A
CountryUS
Kind codeB2
Filing dateMar 9, 2011
Priority dateMar 9, 2010
Publication dateAug 29, 2017
Grant dateAug 29, 2017

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  1. Title

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  2. Abstract

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  4. Key dates

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  5. First independent claim

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Abstract

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In some embodiments, a method to detect acute rejection in allograft from is described. In some embodiments, a method to anticipate an episode of acute rejection in allografts is also described. In some embodiments, a kit for detecting or predicting acute transplant rejection of a transplanted organ is described.

First claim

Opening claim text (preview).

What is claimed is: 1. A method comprising: obtaining a urinary cell sample from a human patient with a renal allograft but without acute cellular rejection of the allograft; quantifying mRNA expression levels of perforin, granzyme B, PI-9, IP-10, CD3, FoxP3, and CXCR3 in the urinary cell sample of the patient; comparing the quantified mRNA expression levels in the urinary cell sample to a corresponding baseline level of mRNA expression of perforin, granzyme B, PI-9, IP-10, CD3, FoxP3, and CXCR3 in urinary cells from a healthy subject or a subject with a non-rejecting renal allograft; detecting upregulation of mRNA expression of perforin, granzyme B, PI-9, IP-10, CD3, and CXCR3 in the urinary cell sample of the patient and initiating treatment with, or providing a modified dose of, an anti-rejection agent to the patient, or detecting upregulation of mRNA expression of perforin, IP-10, FoxP3, and CXCR3 in the urinary cell sample of the patient and initiating treatment with, or providing a modified dose of, an anti-rejection agent to the patient; and obtaining an additional urinary cell sample from the patient after said initiating treatment with, or providing a modified dose of, an anti-rejection agent, and quantifying mRNA expression levels of perforin, granzyme B, PI-9, IP-10, CD3, FoxP3, and CXCR3 in the additional urinary cell sample from the patient. 2. The method according to claim 1 , further comprising comparing log-transformed mRNA expression levels of perforin, granzyme B, PI-9, CD3, FoxP3, and CXCR3 in a urine cell sample from the patient to corresponding log-transformed baseline levels of mRNA expression of perforin, granzyme B, PI-9, IP-10, CD3, FoxP3, and CXCR3 in urine cells from a healthy subject or a subject with a non-rejecting renal allograft. 3. The method according to claim 2 , wherein the log-transformed mRNA levels of perforin, granzyme B, PI-9, IP-10, CD3, FoxP3, and CXCR3 are determined by (i) normalizing mRNA levels to 18S rRNA using a logistic regression model of perforin, granzyme B, PI-9, IP-10, CD3, FoxP3, or CXCR3, or (ii) a weighted combination of at least three log transformed, normalized mRNA levels of perforin, IP-10, FoxP3, granzyme B, PI-9, CD3, or CXCR3 based on a logistic regression model. 4. A method according to claim 1 , further comprising diagnosing future acute rejection when upregulation of mRNA levels is detected in the urine cell sample from the patient. 5. A method according to claim 1 , wherein the method further comprises determining the patient's serum creatinine level in peripheral blood. 6. A method according to claim 1 , wherein the anti-rejection agent is at least one of azathioprine, cyclosporine, FK506, tacrolimus, mycophenolate mofetil, anti-CD25 antibody, antithymocyte globulin, rapamycin, ACE inhibitors, perillyl alcohol, anti-CTLA4 antibody, anti-CD40L antibody, anti-thrombin III, tissue plasminogen activator, antioxidants, anti-CD 154, anti-CD3 antibody, thymoglobin, OKT3, corticosteroid, or a combination thereof. 7. The method of claim 1 , wherein quantifying mRNA expression levels comprises quantifying mRNA levels using one or more probes or primers selected from the group consisting of SEQ ID NO: 1-21, 28, 29 and 30.

Assignees

Inventors

Classifications

  • for diseases caused by alterations of genetic material · CPC title

  • related to diseases not provided for elsewhere · CPC title

  • Prognosis of disease development · CPC title

  • Expression markers · CPC title

  • Transplantation related diseases, e.g. graft versus host disease · CPC title

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What does patent US9746479B2 cover?
In some embodiments, a method to detect acute rejection in allograft from is described. In some embodiments, a method to anticipate an episode of acute rejection in allografts is also described. In some embodiments, a kit for detecting or predicting acute transplant rejection of a transplanted organ is described.
Who is the assignee on this patent?
Suthanthiran Manikkam, Shaked Abraham, Univ Cornell, and 1 more
What technology area does this patent fall under?
Primary CPC classification G01N33/6893. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue Aug 29 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).